Recall Roundup: November 2009

Monday, November 30, 2009

Vita Food Products, Inc. Issues an Alert Announcing Undeclared Wheat in ELF Branded Herring in Sour Cream‏

Vita Food Products, Inc. of Chicago, IL is voluntarily recalling its Elf Branded Herring in Sour Cream product distributed in retail stores in California, Texas, Massachusetts, Maryland, Georgia, Florida, Michigan, Minnesota, North Dakota, and Wisconsin because their labels do not disclose that the product contains wheat. The following product, in the two sizes listed below, is affected by the recall:

SIZE UPC CODE "BEST IF USED BEFORE" DATE
12 oz 0-73302-22111-4 12/APR/10 or earlier
8 oz 0-73302-23111-3 12/APR/10 or earlier

People who are on gluten-free diets run a risk of serious adverse consequences by consuming this product. To date, no illnesses or adverse reactions have been reported in connection with this problem; there is no risk to consumers who do not have a wheat allergy or are not on gluten-free diets.

Vita Food Products, Inc., in its course of its review of its products and labels, discovered that this product was distributed with labels that did not disclose the presence of wheat.

Consumers who are allergic to wheat or have gluten-free diets are urged not to consume the product and to contact Vita Food Products, Inc. at 1-800-989-VITA between the hours of 8:00 am and 5:00 pm Central Time to ask any questions about the product or this Press Release or for a refund of the purchase price of the product.

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Children's Hooded Sweatshirts with Drawstrings Recalled by Allura Imports Due to Strangulation Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Girl's Hooded Sweatshirts

Units: About 3,700

Manufacturer: Allura Imports Inc., of New York, N.Y.

Hazard: The sweatshirts have a drawstring through the hood, which can pose a strangulation hazard to young children. In February 1996, CPSC issued guidelines (pdf) to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper garments, such as jackets or sweatshirts.

Incidents/Injuries: None reported.

Description: This recall involves girl's velour hooded sweatshirts with a zip front. The sweatshirts were sold as a part of a 2-piece set. "Major Diva" is printed on the front of the sweatshirts. The tag on the inside of the sweatshirts reads, "2b REAL." The sweatshirts were sold in hot pink, light pink, ivory and khaki, and in sizes 4, 5/6 and 6X.

Sold exclusively at: Burlington Coat Factory stores nationwide from October 2008 through July 2009 for about $11.

Manufactured in: China

Remedy: Consumers should immediately remove the drawstrings from the sweatshirts to eliminate the hazard, or return the garments to either the place of purchase or to Allura Imports for a full refund.

Consumer Contact: For additional information, contact Allura Imports at (800) 695-4510 between 10 a.m. and 4 p.m. ET Monday through Friday. Consumers can also visit the firm's Web site at www.burlingtoncoatfactory.com

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Team Work Trading Expands Recall of Children's Metal Pendants Due to Risk of Lead Exposure

Wednesday, November 25, 2009

Electrolux ICON(r) and Kenmore PRO(r) Gas Ranges Recalled Due to Carbon Monoxide Poisoning Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Electrolux ICON and Kenmore 30" PRO Gas Ranges

Units: About 900

Manufacturer: Electrolux Home Products Inc., of Augusta, Ga.

Hazard: An incorrect part allows more fuel to pass to the range's oven than can be burned efficiently, causing incomplete combustion and the release of carbon monoxide. This poses a risk of carbon monoxide poisoning to consumers.

Incidents/Injuries: Electrolux has received four reports of incidents involving carbon monoxide being released from the recalled gas range. No injuries have been reported.

Description: The following Electrolux ICON and Kenmore PRO 30" free-standing gas range model and serial numbers are included in this recall. For Electrolux ICON, the model and serial numbers are located on the back of the range. For the Kenmore PRO, the model and serial numbers are located near the base of the range just below the bottom right portion of the oven door and also on the back of the range. Not all serial numbers within these ranges are included in the recall.

Brand: Model
Electrolux ICON Gas Range: E30GF74HPS
Kenmore PRO 30" Gas Range: 790.76913800, 790.76913801

Serial Number Range for all brands/models: NF83000000 - NF93633000

Sold at: Appliance retailers nationwide from August 2008 through October 2009 for between $2,500 and $3,500.

Manufactured in: Canada

Remedy: Consumers should immediately stop using the range's oven and contact Electrolux for the Electrolux ICON or Sears for the Kenmore PRO to schedule a free repair. Consumers can continue to use the cooktop (top burners) and the broiler as well as any clock and/or timer functions.

Consumer Contact: For additional information, contact Electrolux toll-free at (888) 360-8557 between 8 a.m. and 10 p.m. ET Monday through Friday and on Saturdays between 10 a.m. and 3 p.m., or visit the firm's Web site at www.gasrangeorifice.com. Consumers with Kenmore PRO brand ranges should call Sears toll-free at (800) 733-2299 between 8 a.m. and 10 p.m. ET Monday through Saturday.

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Boy's Warm-up Sets Recalled by Fashion Options Due to Strangulation Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Boy's Velour Warm-up Sets

Units: About 5,400

Manufacturer: KT Group Inc., of New York, N.Y.

Hazard: The sweatshirts have drawstrings through the hoods, posing a strangulation hazard to children. In February 1996, CPSC issued guidelines (pdf) (which were incorporated in to an industry voluntary standard in 1997) to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper garments, such as jackets or sweatshirts.

Incidents/Injuries: None reported.

Description: This recall involves boy's hooded sweatshirts style B639BC in colors black, chocolate and charcoal. The velour sweatshirts were sold in sizes S, M, L, or XL and have the name "Beverly Hills Polo Club" on the hangtag and on the center back neck.

Sold at: Burlington Coat Factory nationwide from September 2007 through October 2009. The sweatshirts sold for about $15.

Manufactured in: Bangladesh

Remedy: Consumers should immediately remove the drawstrings from the sweatshirts to eliminate the hazard, or return the garment any Burlington Coat Factory store for a full refund.

Consumer Contact: For additional information, contact Fashion Options collect at (212) 947-2223 between 8:30am and 5:30pm ET Monday through Friday or visit the firm's Web site at www.fashionoptions.com .

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Monday, November 23, 2009

Infant Entrapment and Suffocation Prompts Stork Craft to Recall More Than 2.1 Million Drop-Side Cribs

/PRNewswire/ -- The U.S. Consumer Product Safety Commission (CPSC), in cooperation with Stork Craft Manufacturing Inc., of British Columbia, Canada, today announced the voluntary recall of more than 2.1 million Stork Craft drop-side cribs, including about 147,000 Stork Craft drop-side cribs with the Fisher-Price logo. The recall involves approximately 1,213,000 units distributed in the United States and 968,000 units distributed in Canada.

CPSC urges parents and caregivers to immediately stop using the recalled cribs, wait for the free repair kit, and do not attempt to fix the cribs without the kit. They should find an alternative, safe sleeping environment for their baby. Consumers should contact Stork Craft to receive a free repair kit that converts the drop-side on these cribs to a fixed side.

The cribs' drop-side plastic hardware can break, deform, or parts can become missing. In addition, the drop-side can be installed upside-down, which can result in broken or disengaged plastic parts. All of these problems can cause the drop-side to detach in one or more corners. When the drop-side detaches, it creates space between the drop-side and the crib mattress. The bodies of infants and toddlers can become entrapped in the space which can lead to suffocation. Complete detachment of drop-sides can lead to falls from the crib.

CPSC, Health Canada, and Stork Craft are aware of 110 incidents of drop-side detachment; 67 incidents occurred in the United States and 43 in Canada. The incidents include 15 entrapments; 12 in the U.S. and three in Canada. Four of the entrapments resulted in suffocation: a 7-month-old in Gouverneur, N.Y.; a 7-month-old in New Iberia, La.; a 6-month-old in Summersville, W.Va.; and a 9-month-old in Bronx, N.Y. Included in these incidents are 20 falls from cribs; 12 in the U.S. and eight in Canada. Fall injuries ranged from concussion to bumps and bruises. The cribs involved in these incidents had plastic drop-side hardware that had broken, missing, or deformed claws, connectors, tracks, or flexible tab stops; loose or missing metal spring clips; stripped screws; and/or drop-sides installed upside-down.

This recall involves Stork Craft drop-side cribs and Stork Craft drop-side cribs with the Fisher-Price logo. This recall does not involve any cribs that do not have a drop-side. This recall does not involve any cribs with metal rod drop-side hardware. It involves only those cribs with plastic trigger and one-hand-system drop-side hardware.

This recall includes Stork Craft cribs with manufacturing and distribution dates between January 1993 and October 2009. This recall also includes Stork Craft cribs with the Fisher-Price logo that have manufacturing dates between October 1997 and December 2004. The Stork Craft cribs with the Fisher-Price logo were first sold in the U.S. in July 1998 and in Canada in September 1998. The cribs were sold in various styles and finishes. The manufacture date, model number, crib name, country of origin, and the firm's name, address, and contact information are located on the assembly instruction sheet attached to the mattress support board. The firm's insignia "storkcraft baby" or "storkling" is inscribed on the drop-side teething rail of some cribs. In Stork Craft cribs that contain the "Fisher-Price" logo, this logo can be found on the crib's teething rail, in the manufacturer's instructions, on the assembly instruction sheet attached to the mattress support board, and on the end panels of the Twinkle-Twinkle and Crystal crib models.

Major retailers in the United States and Canada sold the recalled cribs including BJ's Wholesale Club, J.C. Penney, Kmart, Meijer, Sears, USA Baby, and Wal-Mart stores and online at Amazon.com, Babiesrus.com, Costco.com, Target.com, and Walmart.com from January 1993 through October 2009 for between $100 and $400.

The cribs were manufactured in Canada, China and Indonesia.

For additional information, contact Stork Craft toll-free at (877) 274-0277 anytime to order the free repair kit, or log on to www.storkcraft.com.

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Unilever Issues Nationwide Allergy Alert on Undeclared Sulfites in Certain Shedd’s Country Crock® Chilled Side-Dish Products

Unilever United States, Inc., of Englewood Cliffs, NJ, in cooperation with the U.S. Food and Drug Administration (FDA), is voluntarily recalling certain Shedd’s Country Crock® chilled side-dish products because they may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products.

To date, the company has received one report of four family members who had adverse reactions associated with this product.

The product was distributed in retail stores nationwide.

The recall was initiated after the company was notified by the co-manufacturer of the product that an ingredient containing sulfites was inadvertently used in the production of the chilled side-dish products. This issue has been addressed and safeguards have been put into place.

Product description:
Shedd’s Country Crock® Side Dishes DELUXE Cheddar Broccoli Rice, with Best-By dates of NOV 29 09 through to JAN 16 10. The UPC code is 027400218316.

The product comes in a 21-ounce (1 LB 5 OZ / 595 g) plastic tub inside a paperboard sleeve.
Shedd’s Country Crock® Side Dishes DELUXE Four Cheese Pasta, withBest By dates of DEC 05 09 through to JAN 16 10. The UPC code is 027400230875.

The product comes in a 20-ounce (1 LB 4 OZ / 567 g) plastic tub inside a paperboard sleeve.
The UPC code is located on the bottom of the sleeve and the Best-By date is located on the same side of the sleeve and the side of the tub.

In addition to working in cooperation with the FDA, the company is also issuing an alert through the Food Allergy & Anaphylaxis Network.

No other Shedd’s Country Crock® chilled side-dish products are affected by this recall.

Consumers who have purchased the Shedd’s Country Crock® chilled side-dish products are urged to discard them immediately and contact the company at 1-800-457-7086 for a full refund. The Consumer Services Center is open Monday – Friday, 8:30 AM – 6:00 PM ET. A recorded message is available 24/7.

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Saturday, November 21, 2009

Service Smoked Fish Corp. Recalls Smoked Nova Salmon Because of Possible Health Risk

Service Smoked Fish Corp. of Brooklyn, NY, is recalling specific "Use-By" dates and lot codes of Brooklyn's BEST brand SMOKED NOVA SALMON because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may possibly suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

Smoked Nova Salmon was distributed in the greater New York area, New Jersey, Connecticut, and the areas of Baltimore, MD, Los Angeles, CA, and Portland, Oregon. Consumers may have purchased the product from retail food stores.

The Smoked Nova Salmon was vacuum-packed in clear, plastic bags of various size packages including 3 oz., 4 oz., 8 oz., 12 oz., 16 oz. and random weight sides with the brand name "Brooklyn's BEST" appearing on a circular label inside the vacuum bag. A "Use-By" date appears on the bottom of the gold board. Units with "Use-By" dates of 12/03/09 through 12/19/09 are being recalled. The product was also air-packed in bulk boxes. Air-packed units with lot numbers 060 through 043 are being recalled. No other use-by dates or lots numbers are involved in this recall.

No illnesses have been reported to date.

The recall is the result of samplings by the Food and Drug Administration which revealed that the finished products contained the bacteria. The company has ceased the production and distribution of the product. The FDA and the company continue their investigation as to what caused the problem.

Consumers who have purchased the above "Use-By" dates or lot codes of "Brooklyn's BEST" brand SMOKED NOVA SALMON are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718-388-4067, Monday - Friday, 7 am - 3 pm.

Friday, November 20, 2009

Fresh & Easy Neighborhood Market Issues Allergy Alert on Undeclared Pecans in Mislabeled Fresh & Easy Pumpkin Cheesecake Pies

Fresh & Easy Neighborhood Market is voluntarily recalling some fresh&easy™ "Pumpkin Cheesecake Pies" (40 oz.) because they may contain undeclared pecans. Individuals who have allergies to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled product was sold in Fresh & Easy Neighborhood Market stores in California, Nevada and Arizona.

The recall was initiated after it was discovered that a limited number of the fresh&easy™ "Pumpkin Cheesecake Pies" (UPC 5051379033712) were labeled with plain fresh&easy™ "Pumpkin Pie" labels (UPC 5051379008628), which do not declare the presence of pecans. The mislabeled fresh&easy™ Pumpkin Cheesecake pies all carry an "Enjoy by" date of NOV 21 and have been removed from all Fresh & Easy stores.

The fresh&easy™ "Pumpkin Cheesecake Pie" has a crumb topping containing pecans. fresh&easy™ "Pumpkin Cheesecake Pies" which are accurately labeled are not affected by the recall. (see picture of incorrectly labeled product attached)

Customers may return the unused product, empty product containers or present the receipt as proof of purchase of the recalled product to any Fresh & Easy store for a full refund. Consumers who have questions or concerns about this recall should contact the Fresh & Easy 24-hour toll free number at 1 (800) 648-8622.

Salomon USA Recalls Ski Bindings Due to Unexpected Release, Fall Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Alpine Ski Bindings

Units: About 10,000

Importer: Salomon USA, of Ogden, Utah

Manufacturer: Salomon SAS, of France

Hazard: The toe component of the ski bindings could fail to fully secure the ski boot to the ski binding, causing the binding to release unexpectedly. This could cause the skier to lose control or fall and suffer injuries.

Incidents/Injuries: The firm has received two reports of injuries, including a broken leg and a knee injury.

Description: This recall involves the Salomon alpine ski bindings with models LZ 7, LZ 8, LZ 9, LZ 7 SR, LZ 8 SR, LZ 8 SC, and J LZ 9 and the Atomic ski bindings with model Evox 2.8, Evox 2.8+, Evox 2.8++, and FFG 8. "Salomon" or "Atomic" and the respective model number are displayed on the ski bindings. The toe components bear a production date code ending in "8" that can be found on the center plate where the toe of a ski boot contacts the toe component of the bindings.

Sold at: Authorized Salomon USA and Atomic USA ski dealers nationwide from September 2008 through October 2009 for between $90 and $160.

Manufactured in: Romania

Remedy: Consumers should stop using these ski bindings immediately and return the Salomon-brand ski bindings to any authorized Salomon ski dealer, or return the Atomic-brand ski bindings to any authorized Atomic ski dealer, for a free inspection and replacement of the toe component.

Consumer Contact: For additional information, contact the firm toll-free at (877) 789-5111 between 8 a.m. and 4 p.m. MT Monday through Friday; email qualityinfo.usa@salomon-sports.com, or visit the firm's Web sites at www.salomon.com or www.atomicsnow.com

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Stainless Steel Cookware Recalled by Cost Plus World Market Due to Burn Hazard

P&G Voluntarily Recalls Specific Lots of Vicks Sinex Nasal Spray in the United States, Germany and the United Kingdom

The Procter & Gamble Company (NYSE:PG) announced today it is voluntarily recalling three lots of its Vicks Sinex nasal spray in three countries: the United States, Germany and the United Kingdom.

The company said it is taking this precautionary step after finding the bacteria B. cepacia in a small amount of product made at its plant in Gross Gerau, Germany. There have been no reports of illness. However, the bacteria could cause serious infections for individuals with a compromised immune system, or those with chronic lung conditions, such as cystic fibrosis. B. cepacia poses little medical risk to healthy individuals.

P&G detected this problem during routine quality control at the plant and promptly took action. The company’s analysis to date shows this problem is limited to a single batch of raw material mixture involving three lots of product. These three lots were sold only in the United States, Germany and the United Kingdom

P&G is removing the product in question from store shelves and has informed regulatory authorities in the affected countries. P&G said it found the bacteria B. cepacia in a small amount of product from U.S. lot 9239028831 and is conducting testing on the U.K. and German lots that have been produced from the same batch of raw material mixture.

The lot numbers of the products involved are:

Lot #	Country	Product Name
9239028831	United States	Vicks Sinex Vapospray 12-Hour Decongestant Ultra Fine Mist, 15 ml., Nasal Spray
9224028832	United Kingdom	Vicks Sinex Micromist Aqueous Nasal Spray Solution, 15 ml
9224028833	Germany	Wick Sinex Schnupfenspray Dosiersystem, 15 ml

This lot number is listed on both the outer carton and the bottle. Consumers should simply discard the affected product as they would any OTC medicine.

P&G is removing the product in question from store shelves and has informed regulatory authorities in the affected countries. P&G said it found the bacteria B. cepacia in a small amount of product from U.S. lot 9239028831 and is conducting testing on the U.K. and German lots that have been produced from the same batch of raw material mixture.

Anyone who has these specific lots of this product can call P&G for a replacement coupon or refund at the following numbers:

From the United States, please call: 1.877.876.7881 (Hours of operation: Monday - Friday, 9AM - 6PM US ET, Saturday - Sunday, 9AM - 4PM US ET)

From the United Kingdom, please call: 0800.5555.15 (Hours of operation: 19 November, 4PM - 9PM local time and will continue Monday - Friday, 8AM - 6PM local time, Saturday - Sunday, 9AM - 5PM local time)

From Germany, please call: 0800.111.6131 (Hours of operation: 19 November, 4PM - 9PM local time and will continue Monday - Friday, 8AM - 6PM local time, Saturday - Sunday, 9AM - 5PM local time)

Any adverse events with the use of this product and/or quality problems should be reported via the FDA’s MedWatch Program by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch Web site at www.fda.gov/medwatch.

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Thursday, November 19, 2009

Fire and Burn Hazards Prompt Recall of Gas Grills Sold at Lowe's Stores

The U.S. Consumer Product Safety Commission and Health Canada, in cooperation with the firm named below, today announced a voluntary recall of the following products. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Perfect Flame SLG Series Gas Grills

Units: About 663,000 in the United States and about 1,700 in Canada

Importer: L G Sourcing, Inc., of North Wilkesboro, N.C.

Manufacturer: Lucas Innovation Inc., of China

Hazard: The burners can deteriorate causing irregular flames and the lids of some models can catch fire, posing fire and burn hazards to the consumer.

Incidents/Injuries: The firm has received about 40 reports of fires from the burners deteriorating and about 23 reports of the lids catching fire. The firm is aware of one report of an eye injury requiring surgery and 21 incidents of minor burns to the hands, arms or face.

Description: The recalled grills are SLG series "Perfect Flame" brand outdoor propane or natural gas grills. The grills are stainless steel and painted black or gray metal. The model numbers affected by this recall are listed below. The model number can be found in the compartment under the cooking chamber. No other Perfect Flame model numbers are included in this recall.

Model / Replacement Burners / Replacement Lid
SLG2006B / Yes / No
SLG2006BN / Yes / No
SLG2006C / Yes / No
SLG2006CN / Yes / No
SLG2007A / Yes / Yes
SLG2007B / Yes / Yes
SLG2007BN / Yes / Yes
SLG2007D / Yes / No
SLG2007DN / Yes / No
SLG2008A / Yes / Yes

Sold exclusively at: Lowe's retail outlets nationwide from September 2005 through May 2009 for between $200 and $550 (U.S.) and in Canada from December 2007 through May 2009 for between $200 and $250 (CAN).

Manufactured in: China

Remedy: Consumers should immediately stop using the product and contact L G Sourcing to receive free replacement burners and, depending on the model of the grill owned, a free replacement lid.

Consumer Contact: For additional information, contact the firm toll-free at (888) 840-9590 anytime, or visit www.lowes.com

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Gorilla Inc. Recalls EXO-Tech Safety Harness Due to Fall Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: EXO-Tech Safety Harness

Units: About 90

Manufacturer: Gorilla Inc., of Flushing, Mich.

Hazard: The webbing of the waist belt on the safety harness is not routed through the lineman's loop located on the front of the harness near waist level. Since the loops are not properly anchored to the harness webbing but are attached only through stitching not intended to restrain a user during a fall, they that can pull away from the harness when force is applied, leaving the user unrestrained. In addition, the manufacturer of the harness used a previously untested carabiner connector located at the end of the tether at the back of harness, which is the portion of the tether that attaches to the tree.

Incidents/Injuries: No incidents were reported.

Description: This safety harness, used as a fall restraint for hunting, is comprised of two leg straps and two shoulder straps, which connect to a waist belt and padded back support. There is a long, black tether strap at the top rear of the safety harness, which has grey and red accents. The name EXO-Tech is located on the right front shoulder strap and the name Gorilla is located on the left front should strap both in white lettering. Similar to a shirt tag, there is a white manufacturing label on the inside of the back of the harness with the model number 45111 and manufacturing dates, 4/22/2009 or 6/26/2009. These are the only harnesses recalled.

Sold at: Cabelas, Bass Pro and at various sporting goods stores nationwide from May 2009 to August 2009 for about $200.

Manufactured in: Philippines

Remedy: Consumers should immediately stop using the harness and contact Gorilla Inc. to receive a refund.

Consumer Contact: For additional information, contact Gorilla Inc. at (877) 685-7817 between 9 a.m. and 4:30 p.m. ET Monday through Friday or visit the firm's Web site at www.gorillatreestands.com. Consumers can also write to the firm at Gorilla, Inc., P.O. 378, Flushing, MI., 48433 or 3475 Eastman Drive, Flushing, MI. 48433.

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Nassau Candy Issues Nationwide Allergy Alert Because Of Possible Undeclared Allergens on their Tasty Dish Snack Tubs

Nassau CandyIssues Nationwide Allergy Alert Because Of Possible Undeclared Allergens on their Tasty Dish Snack Tubs of Chocolate Almonds, Chocolate Raisins and Sour Neon Worms

Nassau Candy Distributors of Hicksville, New York, is voluntarily recalling possibly unlabeled pegable snack tubs because they contain the following undeclared allergens; Tree Nuts {Almonds}, Soy and Milk and may contain the following undeclared allergens Peanuts, other Tree Nuts {brazil nuts, walnuts, filberts, hazelnuts, pecans, pistachios, macadamia nuts, cashews and coconut}. People who have an allergy to any of these specific types of allergens run the risk of serious or life-threatening allergic reaction if they consume these products.

The Tasty Dish Snack Tubs were distributed and sold nationwide to Bed Bath & Beyond retail stores.

The products come in clear plastic packages that have a triangular front label identifying the Brand: Tasty Dish, the Product Name: Chocolate Almonds, Chocolate Raisins, or Sour Neon Worms and the Net Weight: Chocolate Almonds are 9.75 oz. (276g), Chocolate Raisins are 11oz. (311), and Sour Neon Worms are 9.5 oz. (269g) and they all have a 4” clear film safety shrink band on them. Sku numbers and UPC numbers listed below.

ITEM DESCRIPTION SKU UPC
TUB MLK ALMND 9.75Z 16915300 444444564610
TUB SOUR WORMS 9.5Z 16915289 444444564603
TUB MLK RAISN 11Z 16915335 444444564627

No illnesses have been reported to date in connection with this problem

This voluntary recall was initiated after receiving a report that a small percentage of the tubs in the retail locations were missing the back label. All of the retails stores have been inspected and any tubs that are missing the back labels have been removed from the shelves. Subsequent investigation indicates the problem was caused by a temporary breakdown in the packaging process. The labeling machine that applied the back label which contains the ingredient statement, nutritional information and allergen listing experienced a mechanical malfunction that went undetected by the operator.

Consumers who have purchased these Tasty Dish Snack Tubs and find no back label containing the ingredient statement, nutritional information and allergen listing are urged not to consume the product and to return it to Bed Bath & Beyond for a full refund. Consumers with questions may contact Nassau Candy directly at 516-433-7100 ext 297, Monday – Friday 9 am -4 pm ET.

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Children's Hooded Sweatshirts and Jackets Recalled by Century 21 Promotions, Inc. Due to Strangulation Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Youth Hooded Sweatshirts and Jackets

Units: About 17,000

U.S. Manufacturer/Importer: Century 21 Promotions, of Seattle, Wash.

Hazard: The sweatshirts have a drawstring through the hood which can pose a strangulation hazard to children. In February 1996, CPSC issued guidelines (pdf) to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper garments, such as jackets or sweatshirts.

Incidents/Injuries: None reported.

Description: This recall involves children's sweatshirts and jackets sold in sizes XS - XXL in colors: navy blue, black, brown, pink, red, white, green, grey, blue, yellow, and orange. The recalled garments contain the following embroidered logos: "Montauk," "Avalon," "Stone Harbor," "Cape May," "Sea Isle," "Ocean City," "Alaska," "Nantucket," "Maine," "Long Beach Island," "Lavallette," "Seaside Park," "Newport," "Monterey," "Carmel," "Skaneateles," "1000 Islands," "Block Island" and "Seattle."

Sold at: The following retail and gift shops: Montauk Clothing, Riptide East, Shirt Shops of Cape May, Summer Sweats, Rip Current Sportswear, B&B Dept. Stores, Trapper Jack's, Annie & The Tees, Emporium, Inc., The Trading Co., Mackerel Jack's, Carmel Classics, Rolands, The Ship Gift Shop, Star Dept. Store, Seattle Shirt and Simply Seattle from September 2005 through September 2009 for between $25 and $35. Most stores are located in New England with two stores each in Seattle, Washington and Alaska.

Manufactured in: China

Remedy: Consumers should immediately remove the drawstrings from the sweatshirts to eliminate the hazard, or return the garment to the place of purchase for a full refund.

Consumer Contact: For additional information, contact Century 21 Promotions at (800) 935-2100 between 9 a.m. and 5 p.m. PT Monday through Friday.

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Grand World Recalls "Bobby Chupete" Pacifiers Due to Choking Hazard

Tuesday, November 17, 2009

SNACKS ON RACKS, INC. Issues Nationwide Allergy Alert because of Undeclared Allergens in Their Gourmet Snacks Pack Product Line

Snacks on Racks, Inc. of Parkville, Missouri is recalling products from their line of Gourmet Snacks Packs because they may contain undeclared milk, peanuts, tree nuts, soy, egg, sulfites or wheat. People who have an allergy or severe sensitivity to milk, peanuts, tree nuts, egg, sulfites, soy or wheat run the risk of serious or life-threatening allergic reaction if they consume these products. The complete list of recalled products are listed at the end of this press release.

Gourmet Snack Packs are distributed throughout the continental United States to food service establishments at hospitals, colleges, universities and corporate cafeterias and kiosks. Gourmet Snack Packs are not sold to convenient stores, gas stations, grocery or mass market retailers.

Gourmet Snack Packs are packaged in clear, rectangular-shaped, safety sealed, plastic container with a blue Snacks on Racks label adhered to the top of the product. The retail packaging is not marked with any codes, UPC numbers, or expiration dates. A date code is stickered on the case packaging only. Consumers will be able to distinguish between the recalled product and the correctly-labeled new product because the new product will have the recycling symbol located in the bottom right corner of the label.

No illnesses have been reported to date in connection with this problem.

The recall was initiated when it was discovered that the Snacks on Racks labeling for chocolate raisins did not match the original manufacturer’s allergen statement. Subsequent investigation indicates the problem occurred in the company’s production and packaging processes. Snacks on Racks has implemented new processes to ensure customer safety.

Consumers who have purchased Snacks on Racks Gourmet Snack Packs are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-816-505-9131 between the hours of 8am to 4pm CST Monday through Friday or visit the website at www.snacksonracks.com.

PRODUCT IMPACTED BY THE RECALL:

Product Name Product Weight

Roasted No Salt Almonds 4 oz.
Roasted Salted Almonds 4 oz.
Autumn Mix 5 oz.
Autumn Peanut Mix 5 oz.
Boston Baked Beans 5 oz.
Candy Corn 5 oz.
Caramel Apple Pie Mix 5 oz.
Cherry Slices 5 oz.
Cherry Sour Balls 5 oz.
Chewy Sprees® 5 oz.
Chocolate Almonds 5 oz.
Chocolate Banana Chips 4 oz.
Chocolate Bridge Mix 5 oz.
Milk Chocolate Coffee Beans 5 oz.
Dark Chocolate Coffee Beans 5 oz.
Double Dipped Peanuts 4 oz.
Chocolate Maltballs 3.5 oz.
Chocolate Pretzels 2.5 oz.
Chocolate Raisins 5 oz.
Cinnaberry Breakfast Blend 3 oz.
Cinnamon Bears 5 oz.
Confetti 4 oz.
Dark Chocolate Maltballs 3.5 oz.
Deluxe Mixed Nuts 4 oz.
Energy Mix 4 oz.
Garlic Club Mix 3 oz.
Grape Sour Balls 5 oz.
Gummi Apple O's 4 oz.
Gummi Bears 5 oz.
Gummi Peach O's 4 oz.
Gummi Strawberries 5 oz.
Gummi Worms 4 oz.
Halloween JuJu Pumpkins 5 oz.
2008 Red & Green Sour Balls 5 oz.
Honey Cheddar Mix 2 oz.
Honey Roasted Peanuts 5 oz.
Hot Tamales® 5 oz.
Lemon Drops 5 oz.
Lemonheads® 5 oz.
Mike N Ike® 5 oz.
Mini Red Swedish Fish® 5 oz.
Mini Assorted Swedish Fish® 5 oz.
Natures Harvest 4 oz.
Nik Naks 2 oz.
No Sugar Added Chocolate Raisins 5 oz.
Orange Cranberry Trail Mix 4 oz.
Orange Slices 5 oz.
Peanut Caramel Clusters 4 oz.
Peanut Clusters 4 oz.
Peanut Colada 4 oz.
Select Peanut Mix 4 oz.
Sugar Free Chocolate Peanuts 4 oz.
Salted Cashews 4 oz.
Salted VA Peanuts 4 oz.
Sesame Sensation 3 oz.
Assorted Sour Balls 5 oz.
Sour Bears 5 oz.
Gummi Sour Worms 4 oz.
Soy Energizer Mix 4 oz.
Sour Patch Cherries® 4 oz.
Sour Patch Watermelon® 4 oz.
Sour Patch Kids® 4 oz.
Spicy Club Mix 3 oz.
Strawberry Field Trail Mix 3 oz.
Sunflower Seeds R/S 5 oz.
Toffee Mixed Nuts 4 oz.
Toffee Pecans 4 oz.
Yogurt Almonds 5 oz.
Yogurt Cranberries 5 oz.
Yogurt Pretzels 2.5 oz.
Yogurt Raisins 5 oz.
2008 Holiday Red/Green Pretzel Balls 5 oz.

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RockHard Laboratories Issues a Voluntary Nationwide Recall of Specific Lots of RockHard Weekend Marketed as Dietary Supplement

RockHard Laboratories announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement sold under the name RockHard Weekend (RHW) specific to the following Lot Numbers:

Blister Pack: T12 705 08 (exp: 10/11) / T12 705 09 (exp: 3/12, 8/12)
3ct Bottle: R417 0509 (exp: 09/12)
8ct Bottle: T237-0509 (exp: 06/12)

RockHard Laboratories is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that voluntary lab analysis found that RHW, specific to the above lot numbers, contains sulfoaildenfil, an analogue of Sildenfil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED) making RockHard Weekend an unapproved drug. The active drug ingredient is not listed on the product label.

The undeclared ingredient may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

RockHard Laboratories takes the upmost pride in its quality control by outsourcing production to a certified, independent lab. It is through this outside lab that RockHard Laboratories maintains the highest quality standards possible and can quickly take action. RockHard Laboratories has identified that one of the lab’s raw ingredients, sourced from China, was being unknowingly tainted with sulfoaildenfil. RockHard Laboratories takes this recall very seriously and recommits to the diligent work required in ensuring its products remain free of any potentially unapproved chemicals.

RHW is sold nationwide in single blisters, 3-count and 8-count bottles. RockHard Laboratories advises any customers in possession of RHW to return any unused product for a full refund to the company directly. Customers can call 1.800.562.0543 for instructions on the return and refund process.

RockHard Laboratories is committed to improving its product and avoiding future recall issues by sourcing higher quality raw ingredients and expanding testing. RockHard Laboratories promises its customer the highest possible quality and welcomes the recall process as further evidence of our commitment to our brand, products and consumers.

Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm], by returning the postage-paid FDA form 3500 [which may be downloaded from www.fda.gov/MedWatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA-0178].

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Saturday, November 14, 2009

Conagra Foods Issues Nationwide Allergy Alert on a Limited Number of 15 oz. Tubs of Blue Bonnet Light Spread

ConAgra Foods, in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling a limited number of 15 oz. tubs of Blue Bonnet Spread that were inadvertently mispackaged—the lid is for regular Blue Bonnet Spread and the tub portion describes the product as Blue Bonnet Light Spread. The product inside of the tub is regular Blue Bonnet Spread. As a result, the product tubs do not declare the allergen whey (milk), as an ingredient.

People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume this product. No allergic reactions have been reported.

This issue affects only 1,120 cases of a single lot code of the product. The product UPC on the tub is 27000-00930. The product lid will not have the blue ribbon graphic bearing the word "Light" that is found on the tub portion of the package. The rim of the lid will feature the batch code "2247923200" and a Sell By date of March 18, 2010.

ConAgra Foods became aware of the issue after receiving a report from a store where the tub did not match the lid or the case.

The company is issuing a news release and an alert through the Food Allergy & Anaphylaxis Network (FAAN) (www.foodallergy.org), in an effort to notify any potentially affected consumers.

ConAgra Foods will work with retail customers to ensure that the recalled products are removed from store shelves. In the event that consumers believe they have purchased products affected by this voluntary recall, they should return the product to the store where it was purchased for a full refund. Consumers with questions may call 866-518-4177 (9:00 a.m. to 7:00 p.m. CST daily) or visit www.bluebonnet.com for more information.

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IDS Sports Conducts a Voluntary Nationwide Recall of Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR

IDS Sports announced today that it is conducting a voluntary nationwide recall of five of the company’s dietary supplement products sold under the following names: Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR.

The Food And Drug Administration (FDA) has notified IDS Sports that the recalled products contain the following undeclared substances, which FDA considers to be steroids: “Madol,” “Turinabol,” “Superdrol,” and/or “Androstenedione.”

Acute liver injury is known to be a possible harmful effect of using steroid-containing products. In addition, steroids may cause other serious long-term adverse health consequences in men, women, and children. These include shrinkage of the testes and male infertility, masculinization of women, breast enlargement in males, short stature in children, a higher predilection to misuse other drugs and alcohol, adverse effects on blood lipid levels, and increased risk of heart attack, stroke, and death.

The recalled products listed below were distributed in either black boxes containing blister packs of 60 capsules or white bottles with black labels containing 30 or 60 capsules.
Brand Name Size UPC Lots
Bromodrol 1 box 6 75941 00250 7 All lots
Dual Action Grow Tabs 1 box 6 75941 00252 1 All lots
Grow Tabs 1 bottle 60 capsules 6 75941 00252 1 All lots
Mass Tabs 1 bottle 30 capsules 6 75941 00149 4 Purchased during or after 4/09
Mass Tabs 1 bottle 60 capsules 6 75941 00149 4 Purchased during or after 8/09
Ripped Tabs TR 1 box 6 75941 00162 3 Purchased during or after 12/08
Ripped Tabs TR 1 bottle 60 capsules 6 75941 00162 3 Purchased during or after 12/08

Although no illnesses or adverse events have been reported to the company to date in connection with the products listed above, customers who have these products in their possession should stop using them immediately and contact their physician if they have experienced any problems that may be related to using one or more of the products. Any adverse events that may be related to the use of these products should be reported to the FDA's MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm] or by returning the postage-paid FDA form 3500 [which may be downloaded from www.fda.gov/MedWatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA-0178].

The FDA has been apprised of this recall and IDS Sports is cooperating with the FDA in this recall process.

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Friday, November 13, 2009

GMP Herbal Products, Inc. Issues a Voluntary Nationwide Recall of a Weight Loss Supplement Found to Contain Undeclared Drug Ingredients

GMP Herbal Products, Inc. has been informed by the Food and Drug Administration (FDA) that Pai You Guo, a weight loss dietary supplement, sold and marketed by the firm contains undeclared drug ingredients. FDA lab analyses of dietary supplements distributed by the company were found to contain undeclared sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss; and phenolphthalein, a solution used in chemical experiments and a suspected cancer-causing agent that is not approved for marketing in the United States. The FDA has not approved the Pai You Guo products as drug; therefore the safety and effectiveness of this product is unknown. All lots of the following Pai You Guo product are being recalled. The product is sold either in a box of 30 capsules or a bag of 10 g powder.

The products listed above were sold and distributed nationwide via the internet.

FDA advises that these products pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

No illnesses or injuries have been reported to the company to date in connection with this product.

GMP Herbal Products, Inc. has taken this voluntary action because it is committed to providing accurate information about its products and because of the concern for the health and safety of consumers. GMP Herbal Products, Inc. is working with the FDA in the recall process. It sincerely regrets any inconvenience to customers.

Consumers are advised to destroy the above products or return them to the company’s address in Westminster, CA. Consumers with questions may contact GMP Herbal Products, Inc Tuesday through Saturday 11:00 am to 7:00 pm at 1-866-995-8585.

Any adverse reactions experienced with the use of this product should also be reported to the FDA’s MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at wwww.fda.gov/Safety/MedWatch/default.htm.

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Backpack Blowers Recalled by Homelite Due to Fire Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Homelite Backpack Blowers

Units: About 85,000

Distributor: Homelite Consumer Products Inc., of Anderson, S.C.

Hazard: The fuel tank can leak gasoline, posing a fire hazard to consumers.

Incidents/Injuries: Homelite has received 18 reports of fuel tanks leaking gasoline including one report of minor skin irritation.

Description: This recall involves the Homelite Mighty Lite backpack blowers. The blowers are red and black. The following models are affected by this recall:

Product Model: Manufacturing Date Codes Range
UT08580: ATK1820001 through ATK3659999
UT08580A: ATL1530001 through ATL3669999, ATM0010001 through ATM1749999

The model number and manufacturing date code are printed on the blower's data label which is located on the red plastic housing above the choke knob and adjacent to the fuel tank. Products with a green "dot" on the outside of the package or the letters "CA" embossed on the fuel tank are not included in the recall.

Sold at: Home Depot stores and various retailers of refurbished products including Direct Tools Factory Outlets, CPO Homelite, Gardner, Tap Enterprises, Isla Supply and Heartland America stores nationwide from September 2007 through October 2009 for between $90 and $140.

Manufactured in: China

Remedy: Consumers should stop using their backpack blowers immediately and contact Homelite for the closest dealer location to schedule a free fuel tank replacement.

Consumer Contact: For additional information, contact Homelite Consumer Products, Inc. at (800) 242-4672 between 8 a.m. and 5 p.m. ET Monday through Friday or visit www.homelite.com .

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Treestands Recalled by Gander Mountain Company Due to Fall Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Hang-On Fixed Position Treestands

Units: About 13,000

Importer: Gander Mountain Company, of St. Paul, Minn.

Manufacturer: StrongBuilt, of Waterproof, La.

Hazard: The clasp may open unexpectedly if the strap is fastened incorrectly, causing the treestand and user to fall to the ground.

Incidents/Injuries: Gander Mountain has received two reports of consumers falling while using the treestands: one sustained unspecified injuries and a second person sustained a broken pelvis and broken arm.

Description: Gander Mountain is recalling the 2008 model GMT101 and 2008 model GMT103 Hang-On Fixed Position Treestands. The recalled treestands have wire mesh on the base of the platform to the top of the footrest and a Gander Mountain logo on the front of the seat. In addition, the seat has a camouflage pattern that is branded "AP" and "REALTREE". Model GMT101 has "Steel Hang-On With Foot Rest" printed in large bold print on the exterior of the box and the GMT103 has "Large Steel Hang-On With Foot Rest" printed on the exterior of the box. This recall does not affect the 2009 year models GMT101 and GMT103 Hang-On Fixed Position Treestands manufactured by Rivers Edge.

Sold at: The treestands were sold only at Gander Mountain stores from July 2008 until July 2009. The GMT101 was sold for about $60 and the GMT103 was sold for about $80.

Manufactured in: China

Remedy: Consumers should immediately stop using the recalled treestands and return them to Gander Mountain for a refund, exchange for a 2009 model or a store credit.

Consumer Contact: For additional information, contact Gander Mountain at (888)-542-6337 Monday through Friday between 8 a.m. and 10 p.m and Saturday and Sunday between 9 a.m. and 8 p.m. ET or visit the firm's Web site at www.gandermountain.com .

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Thursday, November 12, 2009

Bicycles Recalled by Easton Sports; Stem Failure Poses Fall Hazard

/PRNewswire/ -- The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Bicycles with EA30 Stems

Units: About 6,400

Importer: Easton Sports, of Scotts Valley, Calif.

Hazard: The bicycle stem can crack and cause the rider to lose control, posing a risk of serious injury if the rider falls.

Incidents/Injuries: The company received a report of a stem breaking, causing a minor injury to the rider.

Description: This recall involves all Raleigh 2007, XXIX 700c MTN, RX1.0, Diamondback 2007, Mission, and Sortie bicycles with EA30 stems. The EA30 stems are black with white-and-gray graphics and feature a four-bolt stem face cap. "EA30" is printed on the stem. EA30 stems sold as aftermarket items are included in this recall.

Sold through: Independent bicycle dealers nationwide from August 2007 through August 2009 for between $500 and $1,200. Aftermarket stems were sold from August 2007 through September 2009 for about $30.

Manufactured in: China

Remedy: Consumers should immediately stop riding the bicycles and contact any authorized Easton Sports for a free replacement stem.

Consumer Contact: For more information, contact Eason Sports toll-free at (866) 892-6059 between 8 a.m. and 5 p.m. CT Monday through Friday or visit the firms' Web site at www.eastonbike.com.

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Wednesday, November 11, 2009

Rechargeable Batteries Used with Touch Panels for Audio/Visual Systems Recalled by AMX Due to Fire and Burn Hazards

Gehl Foods Recalls Nacho Cheese and Chili Sauce Dispensers Due to Fire and Burn Hazards

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Gehl's HOT TOP2 Nacho Cheese and Chili Sauce Dispensers

Units: About 115,000

Manufacturer: Gehl Foods Inc., of Germantown, Wis.

Hazard: The dispenser's fan blade can come into contact with the heater coil, posing fire and burn hazards to consumers.

Incidents/Injuries: Gehl Foods has received 12 reports of the dispenser's fan blade malfunctioning and coming into contact with the heater coil, including one report of a fire that caused property damage. No injuries have been reported.

Description: This recall includes Gehl Food's commercial nacho cheese and chili sauce dispensers with model numbers HT2-04 Single, HT2-04 Dual, and HT2-03 APS with serial numbers HT2 164500 through HT2 299689. The model and serial numbers are located on the back of the dispensers. "Gehl's" is printed on the front of the dispensers.

Sold at: The dispensers were leased to commercial customers nationwide, including concession and food service establishments, from December 2003 through September 2009.

Manufactured in: United States

Remedy: Food establishments and consumers should immediately stop using the recalled nacho cheese and chili sauce dispensers and contact the firm for a free repair by Gehl, or to receive a free repair kit to be installed by the customer.

Consumer Contact: For more information, contact Gehl Foods toll-free at (877) 440-4008 between 8 a.m. and 4:30 p.m. CT Monday through Friday or visit the firms' Web site at www.gehls.com

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Tuesday, November 10, 2009

Maclaren USA Recalls to Repair Strollers Following Fingertip Amputations

Friday, November 6, 2009

Children's Art Easels Recalled by MacPherson's Due to Violation of Lead Paint Standard

Samsung(tm) Over-the-Range Microwaves Recalled Due to Shock Hazard

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Samsung Over-the-Range Microwave Ovens

Units: About 43,000

Importer: Samsung Electronics America Inc., of Ridgefield Park, N.J.

Hazard: If an installation bolt comes in contact with an electrical component inside the unit and the microwave is plugged into an ungrounded outlet, it could create a shock hazard.

Incidents/Injuries: None reported.

Description: The recall involves Samsung 1000 watt over-the-range microwave ovens. The following model and serial numbers are included in this recall:

Affected production lots / Affected Serial Number Range (From serial number To serial number)

All SMH9151x produced from January through May 2009: / xxxxxxxS1xxxxxx to xxxxxxxS5xxxxxx

Some products produced in June were also affected:
SMH9151B / xxxxxxOS600001 to xxxxxxOS600100 and xxxxxxTS600001 to xxxxxxTS601100
SMH9151S / xxxxxxTS600001 to xxxxxxTS601386
SMH9151ST / xxxxxxTS600001 to xxxxxxTS600330
SMH9151STE / xxxxxxTS600001 to xxxxxxTS600330
SMH9151W / xxxxxxOS600001 to xxxxxxOS600200 and xxxxxxTS600001 to xxxxxxTS602055

Sold at: Retail stores nationwide from January 2009 through July 2009 for between $180 and $200.

Manufactured in: Malaysia

Remedy: Consumers should immediately unplug and stop using the recalled product, and contact Samsung to schedule a free repair.

Consumer Contact: For additional information, contact Samsung toll-free at (888) 402-6974 between 9 a.m. and 9 p.m. ET 7 days a week, or visit the firm's Web site at www.samsung.com/otrrecall

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Jelly Belly Issues Allergy Alert on Undeclared Peanuts in 7.5oz cylinder-style packages of 49 Flavors Jelly Belly jelly beans

Jelly Belly Candy Company is recalling 7.5-ounce cylinder-style packages of 49 Flavors Jelly Belly jelly beans because the package is incorrectly labeled. The mislabeled packages failed to list peanut butter and peanut flour in the ingredient statement. People who have an allergy to peanuts or a severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these ingredients.

The Jelly Belly 49 Flavors cylinder packages were shipped to approximately 200 independent stores nationwide from September 29 to October 30, 2009. Product was packaged in a clear 7.5-ounce acetate cylinder with white label on the bottom of the package with lot codes 090925, 090928, 090929 or 091001. UPC code 071567989398

The recall was initiated after the company’s quality control efforts identified the incorrect ingredient statement. No illnesses or allergic reactions have been reported to date. No other candies or packaged candies from Jelly Belly are a part of this recall, and there is no health risk for consumers who are not allergic to peanuts.

Consumers who have a peanut allergy and purchased this product in the last five weeks are urged to return it to Jelly Belly Candy Company, One Jelly Belly Lane, Fairfield, Calif., 94533. Consumers and retailers with questions about the recall should call the Jelly Belly Hotline at 800-522-3267 Monday-Friday 7 am to 5 pm PST

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The Life is Good Company Travel Mugs Recalled Due to Burn Hazard

PetSmart Voluntarily Recalls Dentley's Beef Hooves

PetSmart (NASDAQ: PETM) is voluntarily recalling two Dentley's Beef Hoof products for potential salmonella contamination. The products were manufactured by Pet Carousel, Inc. in Sanger, Calif.

The recalled products include only the following types of Dentley's Beef Hooves purchased between Oct. 2, 2009 and Nov. 3, 2009:

Dentley's Bulk Cattle Hoof UPC# 73725703323
Dentley's 10 Pack Beef Hooves UPC# 73725736055

No other products are included in this recall.

The affected products were shipped from the Pet Carousel plant to three PetSmart distribution centers in Ottawa, Ill.; Groveport, Ohio and Newnan, Ga.; and then shipped directly to certain PetSmart stores. Although the affected product was not shipped to every store, as a precautionary measure PetSmart immediately recalled the product from all of its US stores and instituted a register block to prevent any product from being inadvertently scanned and sold. In addition, PetSmart removed the product from the PetSmart.com Web site and notified PetPerks customers with valid e-mail addresses in the PetSmart database who purchased the affected products.

Salmonellosis is an infection with bacteria called salmonella. Most persons infected with salmonella develop diarrhea, fever, and abdominal cramps 12 to 72 hours after infection. The illness usually lasts four to seven days, and most persons recover without treatment. However, in some individuals, the diarrhea may be so severe that the patient needs to be hospitalized. In these patients, the salmonella infection may spread from the intestines to the blood stream, and then to other body sites and can cause death unless the person is treated promptly with antibiotics. The elderly, infants, and those with impaired immune systems are more likely to have a severe illness.

Many dogs do not show clinical signs of salmonella. However, when they do, they often have diarrhea or other signs of systemic infections.

Customers who purchased the recalled products should discontinue use immediately and return the product to any PetSmart store for a complete refund or exchange. Customers who have concerns about their health or their pet's health should consult a medical professional. For additional information about the recall, customers can visit www.petsmartfacts.com, www.petsmart.com ; www.fda.govor contact PetSmart Customer Service at 1-888-839-9638.

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Adventure Playsets Recall to Repair Backyard Swing Sets Due to Fall Hazard

The U.S. Consumer Product Safety Commission and Health Canada, in cooperation with the firm named below, today announced a voluntary recall of the following products. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Adventure Playsets Wooden Play Sets

Units: About 275,000 in the United States and 6,800 in Canada

Distributor: Adventure Playsets, of Amarillo, Texas

Hazard: The plastic coated lumber on the horizontal ladder (monkey bar/swing beam) can weaken over time due to rotting of the whitewood (spruce, pine and fir species), resulting in a fall hazard.

Incidents/Injuries: Adventure Playsets has received more than 1,400 reports of rotting ladders involving 16 injuries that resulted in nine emergency room visits. The injuries include two arm fractures, lacerations, scrapes, and bruises to children younger than 8 years old. Most of the reported injuries occurred when the swing came out of the monkey bar/ swing beam that had rotted.

Description: This recall involves wooden play sets with swings, slides and ladders. Each set has an overhead monkey bar ladder that acts as both the monkey bar and swing beam, and an end ladder coated with cranberry or green plastic. The instruction manual has the name "Adventure Playsets" and one of the following model numbers printed on the cover.

Durango 1-AP016 and 1- AP018
Yukon 1-AP052
Tacoma 1- AP017 and 1-AP051
El Dorado 1-AP016
Bellevue 1-AP048, and 1-AP012
Dakota 1- AP046
Sherwood 1-AP049
Sedona 1- AP002
Ventura 1-AP008
Madison 1- AP006 and 1-AP015
Belmont 1-AP003

Note: The Bellevue,Tacoma and Durango swing sets were previously recalled due to detaching frames and a fall hazard.

Sold at: Walmart, Toys R Us, Academy Sports, Menards, and Mill stores nationwide, and online at Walmart.com, ToyRUs.com, Willygoat.com and through the DMSI catalog from January 2004 through December 2007 for between $300 and $600.

Manufactured in: United States

Remedy: Consumers should immediately stop using the swing sets and contact Adventure Playsets to receive a replacement kit.

Consumer Contact: For more information, contact Adventure Playsets toll-free at (877) 840-9068 between 8 a.m. and 5 p.m. CT Monday through Friday, or visit the firm's Web site at www.adventureplaysets.com. Consumers can also email the firm at custservice@adventureplaysets.com .

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Wednesday, November 4, 2009

Charleston Cookie Company Issues Allergy Alert on Undeclared Butter in Almond Cookies Produced for Dean & Deluca

Charleston Cookie Company of Charleston, SC is recalling packages of Almond Cookies which were sold as a component of the Dean and Deluca "Americana" cookie tin because the cookies contain undeclared butter (milk).

People who have allergies to milk products run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled Almond Cookies were distributed to Dean & Deluca for resale as part of their "Americana Cookie" collection. The product comes in a 6 ounce, clear plastic package sold with 5 other flavors of cookies in a 36 oz. silver tin. The product bears no code or UPC but was distributed to Dean & Deluca in August 2009 for sale in their catalog and online.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the milk-containing product was distributed in packaging that did not indicate the presence of butter (milk). Investigation indicates that the problem was caused by a temporary breakdown in the company's packaging process. The situation has been rectified by production of a new label with a complete ingredients listing.

Consumers who have purchased the product are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Charleston Cookie Company at 843-762-4185. Business hours are Monday through Friday from 8 am to 5 pm.

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Tuesday, November 3, 2009

Pelican Bay Ltd. Issues Nationwide Allergy Alert on Undeclared Tree Nuts in Caramel Chocolate Truffle Hot Chocolate Mix

Pelican Bay Ltd. of Dunedin, Florida is recalling all their Caramel Chocolate Truffle Hot Chocolate Mix because it may contain undeclared tree nuts. People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

Caramel Chocolate Truffle Hot Chocolate Mix was distributed domestically through direct delivery, mail order and through retail stores. This product is also shipped to Canada, United Kingdom, Japan and the Netherlands. Product distributed between January 2007 and November 2, 2009 is subject to this recall.

Caramel Chocolate Truffle Hot Chocolate Mix is packaged in a cone shape poly bag with a hanging tag attached to the front of the package and SKU# 3204, UPC 94522 01015 on the back of the label.

No illnesses have been reported to date.

The recall was initiated after it was discovered that product containing tree nuts was distributed in packaging that did not reveal the presence of tree nuts.

Consumers who have purchased Caramel Chocolate Truffle Hot Cocoa Mix manufactured by Pelican Bay LTD are urged to call 1-800-826-8982, 9AM to 5 PM EST for information on product returns and replacement.

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BODYBUILDING.COM Is Conducting a Voluntary Nationwide and International Recall of 65 Dietary Supplements That May Contain Steroids

As part of its ongoing cooperation with the Food and Drug Administration ("FDA"), Bodybuilding.com, LLC (the “Company") announced today that it is conducting a voluntary nationwide and international recall of all lots and expiration dates of 65 dietary supplement products (the "Recalled Products") described on the attached list, that were sold through the Company's website, www.bodybuilding.com.

The FDA has informed the Company that it believes that the Recalled Products contain ingredients that are steroids. Specifically, the FDA has advised the Company of its concern that the Recalled Products may contain the following ingredients that are currently classified, or the FDA believes should be classified, as steroids: "Superdrol," "Madol," "Tren," "Androstenedione," and/or "Turinabol." While the Company has not had an opportunity to independently confirm the FDA's concerns that the Recalled Products in fact contain these ingredients, the Company is undertaking this voluntary recall in an abundance of caution.

Acute liver injury is known to be a possible harmful effect of using steroid-containing products. In addition, steroids may cause other serious long-term adverse health consequences in men, women, and children. These include shrinkage of the testes and male infertility, masculinization of women, breast enlargement in males, short stature in children, a higher predilection to misuse other drugs and alcohol, adverse effects on blood lipid levels, and increased risk of heart attack, stroke, and death.

The Company has not received to date any reports of adverse events in connection with the Recalled Products. Because of the possible harmful effects of using products containing steroids, the Company is cooperating with the FDA to conduct a recall of the products the FDA has identified as containing steroids. Prior to agreeing to carry the Recalled Products, the Company received assurances from all of the manufacturers of the Recalled Products that these products were properly classified as dietary supplements in compliance with federal law, meaning that these products did not contain any unlawful ingredient. Customers who have any of the Recalled Products in their possession should stop using them immediately and contact their physician if they have experienced any problems that may be related to taking one or more of the ingredients listed above.

Any adverse events that may be related to the use of the Recalled Products should be reported to the FDA's MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm], by phone [1-800-FDA-1088], or by returning the postagepaid FDA form 3500 [which may be downloaded from www.fda.gov/MedWatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA- 0178].

The Company is committed to providing accurate information about its products. The Company is working voluntarily with the FDA in this recall process.

Consumers should return any unused products purchased on the Company’s site to the Company. For instructions on how to return Recalled Products please call (1-866-236-8417) or e-mail (service@bodybuilding.com) the Company.

RECALLED PRODUCT LIST Brand Name

4Ever Fit D-Drol
Advanced Muscle Science Dienedrone
Advanced Muscle Science Liquidrone UTT
Anabolic Xtreme Hyperdrol X2
APS (aka Advanced Muscle Science) Mastavol
APS (aka Advanced Muscle Science) Revamp
APS (aka Advanced Muscle Science) Ultra Mass Stack
APS (aka Advanced Muscle Science) Ripped Stack
Better Body Sports Finadex
Black China Labs Straight Drol
Black China Labs Straight Phlexed
Body Conditioning Solutions TestraFLEX
Bjorklund Methyldrostanolone
BOSC Enterprises Epi-Tren
BOSC Enterprises Magna Drol
Chaparral Labs Epivol
Chaparral Labs Pheravol-V
Competitive Edge Labs M-Drol
Competitive Edge Labs P-Plex
Competitive Edge Labs X-tren
Diabolic Labs Epio-Plex
Diabolic Labs Finabolic 50
Diabolic Labs Revenge
Ergopharm 6-OXO
Ergopharm 6-OXO Extreme
EST (aka Engineered Sports Technology) MethAnstance
Extreme Labs Susto-Test Depot
Fizogen ON Cycle II Hardcore
G.E.T/ (Genetic Edge Technologies) SUS-500
G.E.T/ (Genetic Edge Technologies) Tren-250
Hardcore Formulations T-Roid
I Force Nutrition 1,4 AD Bold 200
I Force Dymethazine/Reversitol Combo Pack
I Force Reversitol
I Force Nutrition 17a PheraFLEX
I Force Nutrition Dymethazine
I Force Nutrition Methadrol
IDS (aka Innovative Delivery Systems) Bromodrol
IDS (aka Innovative Delivery Systems) Grow Tabs TR
IDS (aka Innovative Delivery Systems) Mass Tabs
IDS (aka Innovative Delivery Systems) Oxodrol Pro
IDS (aka Innovative Delivery Systems) Ripped Tabs TR
IDS (aka Innovative Delivery Systems) Rapid Release
Ripped Tabs
Kilo Sports Massdrol
Kilo Sports Phera-Mass
Kilo Sports Trenadrol
Monster Caps Monster Caps
Myogenix Spawn
Nutra Coastal D-Stianozol
Nutra Coastal H-Drol
Nutra Coastal MDIT
Nutra Coastal S-Drol
Nutra Coastal Trena
Performance Anabolics Methastadrol
Performance Anabolics Tri-Methyl X
Purus Labs E-pol Inslinsified
Purus Labs Nasty Mass
Rage RV2
Rage RV3
Rage RV4
Rage RV5
Redefine Nutrition Finaflex 550-XD
Redefine Nutrition Finaflex Ripped
Transform Supplements Forged Extreme Mass
Transform Supplements Forged Lean Mass

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Sunday, November 1, 2009

Alexia Foods issues nationwide allergy alert and product recall on its Alexia Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds frozen potatoes

Alexia Foods issues nationwide allergy alert and product recall on its Alexia Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds frozen potatoes due to undeclared pine nut allergen

Alexia Foods, Inc, Kennewick, WA, in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling packages of its Alexia – Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds (frozen seasoned potato wedges) for an undeclared allergen, pine nuts. People who have an allergy or severe sensitivity to pine nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The product was distributed to retail stores nationwide.

The affected product, Alexia – Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds, is packaged in 15 oz. white poly bags with a teal-colored graphic banner and pictures seasoned potato wedges on the front bag panel. This voluntary recall is limited to only packages of Alexia – Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds bearing the following Sell By dates (shown below) printed on the upper left back panel of the poly package with the UPC # 34183 00108. No other Alexia frozen or shelf stable products are affected.

Sell By 5385050811 Sell By 5385050911
Sell By 5385051011 Sell By 5385051111

The product was produced with packaging that does not declare pine nuts in the product. Alexia Foods has taken the precautionary measure of notifying the U.S. Food and Drug Administration (FDA) and is voluntarily recalling about 9,000 cases of the product.

Alexia Foods will work with retail customers to ensure that the recalled products are removed from store shelves. In the event that consumers believe they have purchased products affected by this voluntary recall, they should return the product to the store where it was purchased for a full refund. Consumers with questions may call 1-866-518-0894 or visit www.alexiafoods.com for more information.

Alexia Foods is also issuing an alert through the Food Allergy & Anaphylaxis Network (FAAN) in an effort to notify any potentially affected consumers.

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Allergy Alert on Possible Undeclared Soy Protein in Some Kroger, Great Value and Wholesome Farms Products

Allergy Alert on Possible Undeclared Soy Protein in32-ounce Great Value Half & Half, 32-ounce Great Value 36% Heavy Whipping Cream, 32-ounce Kroger brand 36% Heavy Whipping Cream, and 64-ounce Wholesome Farms Chocolate Ice Cream Mix

Morningstar Foods is voluntarily recalling 32-ounce Great Value Half & Half, UPC 6 05388 187 16 1, item code 1871600, plant code 21-031; 32-ounce Great Value 36% Heavy Whipping Cream, UPC 6 05388 187 18 5, item code 1871800, plant code 21-031; 32-ounce Kroger brand 36% Heavy Whipping Cream, UPC 0 11110 438 28 7, item code 4382900, plant code 21-031; and 64-ounce Wholesome Farms Chocolate Ice Cream Mix, UPC 0 74865 57 983 4 (if purchased in a multi-pack, the UPC code is 1 00 74865 57983 1), item code 5798300, plant code 21-031 because these products may contain soy protein. The individual cartons are printed with a “use by” date of December 16, 2009 for the Great Value items; December 16 and 17, 2009 for the Kroger item; and January 7, 2010 for the Wholesome Farms item. Consumers can find the expiration date and the plant code on the top of the gable top package. The UPC code will either be located on the back or the side panel of the gable top carton. No other Great Value, Kroger or Wholesome Farms products are involved in this recall.

People who have a known allergy to soy protein may have a reaction to these products. Common symptoms of an allergic reaction include hives, swelling, shortness of breath, wheezing, vomiting and stomach or intestinal upset. If a consumer experiences any of the above symptoms, they should see their healthcare professional immediately. If left untreated, severe allergic reaction can be fatal. No reactions have been reported. The problem was discovered when consumers reported off-taste in some of these products.

The affected product was distributed to retail outlets in the following states: Alabama, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, Nebraska, New York, North Carolina, North Dakota, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Vermont, Virginia, West Virginia and Wisconsin. Morningstar Foods’ sales team is working with distributors to actively recover any affected product remaining on store shelves.

HOW TO IDENTIFY THE RECALLED PRODUCT
This recall includes only the products listed below. Each product is sold in a cardboard gable-top carton. Consumers can find the expiration date and the plant code on the top of the gable top package. The UPC code will either be located on the back or the side panel of the gable top carton. No other Great Value, Kroger or Wholesome Farm products are involved in this recall.

* 32-ounce Great Value Half & Half: UPC 6 05388 187 16 1, item code 1871600, plant code 21-031, “use by” date of December 16, 2009
* 32-ounce Great Value 36% Heavy Whipping Cream: UPC 6 05388 187 18 5, item code 1871800, plant code 21-031, “use by” date of December 16, 2009
* 32-ounce Kroger brand 36% Heavy Whipping Cream: UPC 0 11110 438 28 7, item code 4382900, plant code 21-031, “use by” date of December 16 and 17, 2009
* 64-ounce Wholesome Farms Chocolate Ice Cream Mix: UPC 0 74865 57 983 4, item code 5798300, plant code 21-031, “use by” date of January 7, 2010 (if purchased in a multi-pack, the UPC code is 1 00 74865 57983 1)

The Company apologizes for any inconvenience to its customers. Consumers who purchased the product may return it to the place of purchase for a full refund or exchange. Consumers with questions can contact the Company at 800-854-3243 from 8 a.m. – 5 p.m. Central Time.

The Food and Drug Administration has been notified of this recall.

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