Friday, July 30, 2010

Nutraloid Labs Inc. Conducts Voluntary Nationwide Recall of Two Dietary Supplements Found to Contain Undeclared Drug Ingredient

Nutraloid Labs Inc. announced today that it is conducting a voluntary nationwide recall of two dietary supplement products sold under the names: ejaculoid XXTREME and stimuloid II.

Nutraloid Labs Inc. has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis of ejaculoid XXTREME, Lot 79935, and stimuloid II, Lot 79936, by the FDA found that the products contain sulfoaildenafil, similar in structure to Sildenafil. Sildenafil is an active ingredient of an FDA-approved drug for male Erectile Dysfunction (ED), making these products unapproved drugs. The active drug ingredient is not listed on the product label. The undeclared ingredient 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.

The recalled products listed below were distributed in black plastic bottles to distributors and via internet sales.

Brand Name Size Lot UPC
Ejaculoid XXTREME 30 Capsules/Bottle 79935 12/12 8 04879 17868 2
Stimuloid II 30 Capsules/Bottle 79936 12-12 8 04879 17867 5

No illnesses have been reported to the company to date in connection with these products.

Customers who have any of the above 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 these products.

Consumers and healthcare professionals should report any adverse events that may be related to the use of the above products to the FDA's Med Watch Adverse Event Reporting Program online at www.fda.gov/medwatch/report.htm9, by phone 1-800-FDA-1088, or by returning the postage-paid FDA form 3500 which may be downloaded from www.fda.gov/MedWatch/getforms.htm10 by mail to FDA Med Watch, HF-2, 5600 Fishers Lane, Rockville, MD 20852-9787 or fax to 1-800-FDA-0178.

Nutraloid Labs Inc. is conducting this recall with the knowledge of the FDA. Consumers should return any unused product to the place of purchase or contact Nutraloid Labs Inc. directly at 1-772-291-7510, Monday – Friday, 10 am to 4 pm EDT.

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Wednesday, July 28, 2010

Voluntary Recall of PreserVision® Eye Vitamin AREDS 2 Formula in the United States

Bausch + Lomb is conducting a voluntary recall of its PreserVision® Eye Vitamin AREDS 2 Formula with Omega 3 soft gels, only available within the United States.

Bausch + Lomb chose to initiate this recall based on a small number of reports predominantly within a specific age group, age 70 and older, who reported difficulty swallowing or a choking sensation when taking the soft gel.

The voluntary recall is limited only to the United States; it does not affect locations in Europe, the Middle East or Asia-Pacific regions. The PreserVision Eye Vitamin AREDS 2 Formula with Omega 3 is the only supplement affected in the recall; all other PreserVision and Ocuvite® supplements, soft gels and tablets, remain on the market.

To clarify, the formulation of PreserVision Eye Vitamin AREDS 2 Formula with Omega 3 is safe. While many of our customers can comfortably swallow the supplement, we believe the design of the soft gel requires further consideration. Our customers are our top priority, and we want to ensure they have a supplement which is comfortable to use on a daily basis.

Bausch + Lomb expects to release an AREDS 2 formulation in a smaller soft gel which will be dosed twice per day, two pills per dose. This immediate redesign is expected to be available to customers by later this year.

We have directly contacted U.S. retailers who have been shipped this product to initiate the recall and inform them of the steps they should take to return the product to us. We have also contacted eye care professionals to alert them of the recall.

We are asking consumers who currently have the PreserVision Eye Vitamin AREDS 2 Formula with Omega 3 to return the product to Bausch + Lomb. Even if consumers are comfortable swallowing the soft gel, we urge them to return the product.

Consumers who have this product in their home should call our customer service center for instructions on returning and reimbursement: 1-800-553-5340. Bausch + Lomb’s customer service line is open to consumers 9am-5pm EST Monday through Friday.

AFFECTED PRODUCT DETAILS:

Lot Numbers:
0923BK103, 0924BK103, 0924BK103A, 0925BK103A, 0926BK103A, 0927BK103A, 0928BK103A, 0929BK103A, 0930BK103A

UPC Code: 24208 62584

Expiration Date: 08/31/2011

Packaging and Dosage:
PreserVision Eye Vitamin AREDS 2 Formula with Omega 3 soft gels are packaged in 60 count bottles. The current dosage for the AREDS 2 formulation is two soft gels per day.

Bausch + Lomb chose to initiate this voluntary recall because we feel it is in the best interest of our patients to make certain they have a high-quality product which is comfortable to use on a daily basis.

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Tuesday, July 27, 2010

Brine Recalls VIP Lacrosse Gloves Due to Violation of Lead Paint Standard

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 consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Youth and Adult Brine VIP Lacrosse Gloves

Units: About 7,000 in the United States and 30 in Canada

Manufacturer: Brine, a division of Warrior Sports Inc., of Warren, Mich.

Hazard: Screen printing ink used on the silver triad logo on the back of the glove contains excessive levels of lead, violating the federal lead paint standard.

Incidents/Injuries: None reported.

Description: This recall involves black and white Brine VIP lacrosse gloves sold in three sizes: 10, 12 and 13 inches. The name "Brine" is printed in white and a silver triad symbol is printed on the back of the glove on the wrist cuff. The following lacrosse gloves are involved in this recall:

- Model Number: LGLVIP03-618983164529 / Size: 13 inches
- Model Number: LGLVIP02-618983164505 / Size: 12 inches
- Model Number: LGLVIP00-618983164543 / Size: 10 inches

Sold at: Sporting goods stores nationwide between July 2009 and June 2010 for about $50.

Manufactured in: Vietnam

Remedy: Consumers should immediately stop using the gloves and contact Brine for a replacement or refund.

Consumer Contact: For additional information, contact Brine toll-free at (888) 542-8834 between 8 a.m. and 10 p.m. ET Monday through Friday, or visit the firm's website at http://www.brine.com/recall

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Friday, July 23, 2010

DeBoles® Nutritional Foods, Inc. Voluntarily Recalls One Lot Code of DeBoles® Kids Only! Gluten Free Tubettini Corn Pasta Due to the Presence of an Undeclared Allergen, Lot Code 30JUN11D1

DeBoles Nutritional Foods, Inc. announced that it is recalling one lot code of DeBoles® Kids Only! Gluten Free Tubettini Corn Pasta because it may contain undeclared whole wheat alphabet pasta. People who are allergic to wheat run the risk of an allergic reaction, which may be serious or life-threatening if they consume the recalled product.

The recalled lot was distributed to stores nationwide and through internet orders.

The product comes in a cardboard box, 8.5 ounce, with a clear plastic window. The expiration lot code is on the top of the box and the UPC Code 087336638305 appears on the bottom of the box. No other lot codes are affected. This recall only affects:

Deboles kids only! gluten free tubettini corn pasta

Lot code:        30JUN11D1

No illnesses have been reported in connection with this product. It appears that certain product boxes in lot code 30JUN11D1 may contain whole wheat alphabet pasta mixed with the gluten-free tubettini corn pasta in packaging that did not declare wheat as an allergen and, as a result, the product is being recalled. The alphabet pasta is clearly visible and is a darker color and characteristic alphabet shape compared to the yellow corn small-tube pasta.

Consumers who have purchased 8.5 ounce packages of DeBoles® Kids Only Gluten Free Tubettini Corn Pasta with Lot Number 30JUN11D1 are urged to return such packages to their place of purchase for a full refund. Consumers with questions may contact the company at 1-800-434-4246 during extended hours from Monday to Friday 9 am to 9 pm EDT, and on Saturday and Sunday from 10 am to 6 pm.

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Thursday, July 22, 2010

J & H Besta Corp. Issues a Voluntary Nationwide Recall of Joyful Slim Herb Supplement Found to Contain an Undeclared Drug Ingredient

J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Joyful Slim Herb Supplement distributed by the company was found to contain undeclared Desmethyl Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved this product, therefore the safety and effectiveness of the product is unknown.

FDA advises that this product poses 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.

Joyful Slim Herb Supplement is marketed as a Natural Herb for Weight Loss. Joyful Slim Herb Supplement is packaged in plastic bottles containing 30 capsules per bottle and bears UPC 8 97966 00200 7. The affected lot/code being recalled is 101408. The product was sold to distributors and retail stores nationwide and via internet sales.

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

J & H Besta Corp. is taking this voluntary action because of the concern for the health and safety of consumers. The company has discontinued distribution of Joyful Slim. It sincerely regrets any inconvenience to our customers.

Consumers should not consume the Joyful Slim Herb Supplement and should return it immediately to the place of purchase for a full refund. Consumers with questions should contact Jason Wang at 877-547-5468, Monday through Friday, 10:00 am to 5:30 pm, EDT.

Any adverse reactions experienced with the use of this product may be reported to the FDA's MedWatch Safety Information and Adverse Event Reporting Program online [at www.fda.gov/MedWatch/report.htm], by phone 1-800-332-1088 [1-800-FDA-1088], or by returning the postage-paid FDA form 3500 [which may be downloaded from the MedWatch "Download Forms" page], by mail [to address on the pre-addressed form] or fax [1-800-FDA-0178].

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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Atico International USA Recalls Bamboo Torches Due to Laceration 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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Bamboo Torches

Units: About 324,000 units

Distributor: Atico International USA Inc., of Fort Lauderdale, Fla.

Hazard: The fuel canister that holds the wick of the torch has a sharp edge inside the lip of the opening that poses a laceration hazard when consumers try to remove the wick.

Incidents/Injuries: The firm has received five reports of lacerations to fingers, including one that required stitches. Four of the injuries occurred when consumers were trying to retrieve a wick that had fallen into the canister.

Description: This recall involves bamboo torches that have a black metal canister with a smooth black metal lid. The torches are used to light outdoor gatherings. The following are the UPC numbers included in this recall. The UPC number can be found on the tag.

Model Number / UPC Number / Distribution Date / Description

A26I0683 / 1249584485 / February 2008 / 5"-6" long black metal canister with a black metal lid, a wick and a wick cap made of either dark metal or wood. The canister is wrapped with red bamboo.

A26I0037 / 1249597837 / Between April 2008 - March 2009 / 5"-6" long black metal canister with a black metal lid, a wick and a wick cap made of either dark metal or wood. The canister is wrapped with red bamboo.

A26I0943 / 639277779885 / February 2009 / 5"-6" long black canister with a black metal lid, a wick and no wick cap. The product is sold in packages of 2. The canister is wrapped with light beige and dark brown intertwined bamboo.

Sold at: CVS/Pharmacy, Rite Aid and Dollar Tree/Deals$ stores from February 2008 through March 2010 for between $3 and $5.

Manufactured in: China

Remedy: Consumers should immediately stop using the recalled torches and contact Atico International USA for instructions on obtaining a full refund.

Consumer Contact: For additional information, contact Atico International USA toll-free at (866) 448-7856 between 9 a.m. and 5 p.m. ET Monday through Friday or visit the company's website at www.aticousa.com

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Tuesday, July 20, 2010

Good Health, Inc. Issues a Nationwide Voluntary Recall of Product Marketed as Dietary Supplement

Good Health, Inc. announced today that it is conducting a voluntary nationwide recall of the company's dietary supplement Vialipro for sexual enhancement sold under the Lot Numbers listed below.

This product is currently being sold as a dietary supplement throughout the U.S. Good Health, Inc. is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that a lab analyses found that the product tested from certain batches of Vialipro contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED) making this product an unapproved drug. The active drug ingredient is not listed on the product label.

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

Vialipro Sold Under the Following Lot Numbers

Lot Number
80409
Capsules, 10 Count
All Dates
80661
Capsules, 10 Count
All Dates
 81146
Capsules, 10 Count
All Dates
90132
Capsules, 10 Count
All Dates
90265
Capsules, 10 Count
All Dates
90587
Capsules, 10 Count
All Dates
90826
Capsules, 10 Count
All Dates
91065
Capsules, 10 Count
All Dates
00197
Capsules, 10 Count
All Dates
'00347
Capsules, 10 Count
All Dates


Laboratory analysis identified that one of the raw ingredients was tainted with Sulfoaildenafil. Good Health, Inc. takes this recall very seriously and is committed to the diligent work required to ensuring its products remain free of any potentially unapproved chemicals. We take the utmost pride in our product quality control and have the highest regard for our customer's health.

We urge consumers who have purchased Vialipro to discontinue its use and return it to Good Health, Inc.. Customers can call Good Health, Inc. at 1 (866) 607-0338 Monday through Friday from 9:00 am - 5:00 pm MST for instructions on the return and refund process.

Distributors are advised to stop selling Vialipro and contact Good Health, Inc. at 1 (866) 607-0338 for further instructions.

It is the position of Good Health, Inc. that we did not in any way knowingly or intentionally violate the law with regard to the distribution of these products.

Adverse reaction or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program online, by regular mail, or by fax. Online: www.fda.gov/MedWatch/report.htm.9 Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at www.fda.gov/MedWatch/getforms.htm10. Mail to address on the pre-addressed form. Fax: 1-800-FDA-0178.

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J & H Besta Corp. Issues a Voluntary Nationwide Recall of Slim- 30 Herb Supplement Found to Contain an Undeclared Drug Ingredient

J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Slim-30 Herb Supplement distributed by the company was found to contain undeclared N-Desmethyl Sibutramine and traces of Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved this product, therefore the safety and effectiveness of the product is unknown.

FDA advises that this product poses 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.

Slim-30 Herb Supplement is marketed as a Natural Herb for Weight Loss. Slim-30 Herb Supplement is packaged in plastic bottles containing 30 capsules per bottle and bears UPC 8 31457 005009 2. The affected lot/code being recalled is 032009. The product was sold to distributors and retail stores nationwide and China and via internet sales.

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

J &H Besta Corp. is taking this voluntary action because of the concern for the health and safety of consumers. The company has discontinued distribution of this affected product lot. It sincerely regrets any inconvenience to our customers.

Consumers should not consume the Slim-30 Herb Supplement and should return it immediately to the place of purchase for a full refund. Consumers with questions should contact Jason Wang at 516-735-1436, Monday through Friday, 10:00 am to 5:30 pm, EDT.

Any adverse reactions experienced with the use of this product may be reported to the FDA's MedWatch Safety Information and Adverse Event Reporting Program online [at www.fda.gov/MedWatch/report.htm9], by phone 1-800-332-1088 [1-800-FDA-1088], or by returning the postage-paid FDA form 3500 [which may be downloaded from the MedWatch "Download Forms10" page], by mail [to address on the pre-addressed form] or fax [1-800-FDA-0178].

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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Friday, July 16, 2010

Baja Motorsports Recalls Mini Bikes and Go-Carts 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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Baja Motorsports Mini Bikes and Go-Carts

Units: About 308,000

Importer: Baja Inc., d/b/a Baja Motorsports, of Phoenix, Ariz.

Hazard: The gas cap can leak or detach from the fuel tank on the recalled mini bikes and go-carts, posing a fire and burn hazard to consumers. In addition, the throttle can stick due to an improperly positioned fuel line and throttle cable, posing a sudden acceleration hazard to consumers.

Incidents/Injuries: The firm has received at least 9 reports of the gas caps leaking and detaching, including one report of a serious burn injury to a child. The firm has also received 25 reports of stuck throttles possibly due to the fuel line and throttle cable being improperly attached with injuries to the face and other parts of the body reported.

Description: This recall involved Baja Motorsports mini bikes with model numbers beginning with HT65, MB165, WR65, MB196, DB30, WR90 and DR90 and go-carts with model numbers BB65, SD65, DN65 and TR65. The model number is located on the mini bikes' fenders and/or decorative fuel tank and on the go-carts' roll cage. They both have black plastic gas caps.

Sold at: Various mini bike and go-cart retailers nationwide from November 2004 through June, 2010 for between $200 and $2000. They were also available from the following web sites: Costco.com; Amazon.com; toysrus.com; northerntool.com; sears.com; and kmart.com.

Manufactured in: China

Remedy: Consumers should immediately stop using the recalled mini bikes and go-carts and contact Baja Motorsports for a free replacement gas cap and to schedule a free repair of the fuel line and throttle cable.

Consumer Contact: For additional information, contact Baja Motorsports toll-free at (888) 863-2252 between 10 a.m. and 7 p.m. ET Monday through Friday or visit the firm's website at www.bajamotorsports.net

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Feline’s Pride Expands Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination

Feline’s Pride is expanding its July 1, 2010 voluntary recall of Feline’s Pride Raw food with ground bone for cats and kittens, Natural Chicken Formula, Net Wt. 2.5 lbs. (1.13 kg., 40 oz.) produced on 6/10/10 to include the product produced on 6/21/10, because it may be contaminated with Salmonella. People handling raw pet food can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with the raw pet food or any surfaces exposed to the product.

When consumed by humans, Salmonella can cause an infection, salmonellosis. The symptoms of salmonellosis include nausea, vomiting, abdominal cramps, minimal diarrhea, fever, and headache. Certain vulnerable populations, such as children, the elderly, and individuals with compromised immune systems, are particularly susceptible to acquiring salmonellosis from such pet food products and may experience more severe symptoms.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

The product is packaged in uncoded plastic containers and sold frozen to private consumers nationwide. Once thawed, the pet food has a shelf life of about 1 week. The firm manufactures the pet food by an as-ordered basis. This expansion of the recall affects those orders placed and shipped from June 21 through June 26, 2010 (produced on 6/21/10).

The firm and FDA are investigating this matter to determine the source of this problem, and will take any additional steps necessary to protect the public health.

To date, both the firm and the FDA have received no reports of Salmonella infection relating to this product.

People who are experiencing the symptoms of Salmonella infection after having handled the pet food product should seek medical attention, and report their use of the product and illness to the nearest FDA office.

People should thoroughly wash their hands after handling the pet food – especially those made from raw animal protein such as meat or fish -- to help prevent infection. People may risk bacterial infection not only by handling pet foods, but by contact with pets or surfaces exposed to these foods, so it is important that they thoroughly wash their hands with hot water and soap.

Since certain vulnerable populations, such as children, the elderly, and individuals with compromised immune systems, are particularly at risk from exposure they should avoid handling this product.

Consumers with questions should contact the company at (716) 580-3096, Monday -Friday from 10 am - 4 pm EDT.

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Thursday, July 15, 2010

Child's Death Prompts Recall to Repair Portable Playard Tent by Tots in Mind Due to Strangulation Hazard

/PRNewswire-/ -- The U.S. Consumer Product Safety Commission (CPSC), in cooperation with Tots in Mind Inc., of Salem, N.H., is announcing the voluntary recall today of about 20,000 (and 85 in Canada) Cozy Indoor Outdoor Portable Playard Tents Plus Cabana Kits.

Clips that attach the tent to the top of the playard can break or be removed by a child. A child can lift the tent and become entrapped at the neck between the rigid playard frame and the metal base rod of the tent, posing a strangulation hazard.

CPSC is aware of a death of a 2-year-old boy in December 2008 in Vinalhaven, Maine. The boy was found hanging with his neck entrapped between the playard frame and the metal base rod of the tent that had been partially tied by pieces of nylon rope and partially attached by clips. The tent was tied to the playard because the child was able to pop off the clips. Apparently, the child became entrapped while attempting to climb out of the playard. In three other incidents, children were able to remove one or more clips and place their necks between the tent and the playard. The children were not injured.

The dome-shaped white-colored mesh tent is designed to fit over playards as small as 28 inches by 40 inches or as large as 31 inches by 44 inches to contain a child. There are 12 plastic clips to secure the base of the tent to the top rail of the playard through button holes along the bottom of the tent. The tent has a zippered side for putting in and taking out the child.

The cribs were made in China and sold at Walmart, Amazon.com and various baby and children's stores nationwide from January 2005 through February 2010 for about $60.

Consumers should immediately stop using the playard tents and contact Tots in Mind to get free replacement clips. Replacement clips will be available in late August or early September 2010. Contact Tots in Mind toll-free at (800) 626-0339 between 8 a.m. and 5 p.m. ET Monday through Friday or visit the firm's website at www.TotsinMind.com.

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Muddy Outdoors Recalls Climbing Sticks 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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: 2009 Muddy Outdoors tree climbing sticks

Units: Approximately 2,550

Manufacturer: Muddy Outdoors, of Camdenton, Mo.

Hazard: Bolts that secure the cam locs to the frame of these climbing sticks that retains the rope around the tree can break, allowing the cam locs to detach from the frame. This causes the retaining rope to detach and the climbing stick to release from the tree, posing a fall hazard to the user.

Incidents/Injuries: CPSC has received two reports of bolts breaking on a climbing stick. No reports of injuries.

Description: The recalled climbing sticks are used for climbing a tree and include 2009 year Model 70301 - Muddy Outdoors climbing stick (a 20 inch single climbing stick) and 2009 year Model 70304 - Muddy Outdoors climbing stick (4 pack of 20-inch climbing sticks). The year and model number is printed on a label on the front of the main vertical frame of the climbing stick just below the two cam locs.

Sold at: Directly from Muddy Outdoors via Internet/telephone sales and other outdoor sports retailers nationwide from July 2009 through April 2010 for about $35 (model 70301) and about $130 (model 70304).

Manufactured in: China

Remedy: Consumers should immediately stop using these climbing sticks and return the climbing sticks to Muddy Outdoors for a refund, exchange or manufacturer's credit.

Consumer Contact: For additional information contact Muddy Outdoors toll-free at (877) 366-8339 between 8:30 a.m. and 4 p.m. CT Monday through Friday or visit the firm's website at www.gomuddy.com or e-mail the firm at info@gomuddy.com

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Wednesday, July 14, 2010

Tween Brands Recalls Children's Metal Jewelry Due to High Levels of Cadmium

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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Metal Necklaces, Bracelets and Earrings

Units: About 137,000

Importer/Distributor: Tween Brands Inc., of New Albany, Ohio

Hazard: The children's metal jewelry contains high levels of cadmium. Cadmium is toxic if ingested by children and can cause adverse health effects.

Incidents/Injuries: None reported

Description: This recall involves 19 different styles of children's metal necklaces, bracelets and earrings. Styles and shapes of the jewelry include hearts, heart locks, butterflies, cupcakes, peace signs and crowns. Some jewelry contains the words "Best," "Friends" or "Forever" and/or "BFF." Only style numbers listed below are included in this recall. The style number is included on the jewelry's packaging.

- Justice Butterfly Earrings Style #5837
- Justice Cupcake Earrings (Dark Pink) Style #5814
- Justice Cupcake Earrings (Brown) Style #5467
- Justice Cupcake Earrings (White) Style #5469
- Justice Cupcake Earrings (Light Pink) Style #5758
- Justice Cupcake Earrings (Light Blue) Style #5759
- Justice BFF Bracelet Style #3609
- Justice BFF Bracelet Style #5778
- Justice BFF Bracelet Style #5782
- Justice Heart Lock Necklace Style #6905
- Justice Cupcake Necklace (Royal Blue) Style #6936
- Justice Cupcake Necklace (White) Style #6929
- Justice Cupcake Necklace (Dark Pink) Style #6937
- Justice Cupcake Necklace (Light Blue) Style #6928
- Justice Cupcake Necklace (Light Pink) Style #6927
- Justice BFF Necklace Style #6904
- Justice Heart Necklace Style #6907
- Justice Crown Necklace Style #6908
- Justice Peace Sign Necklace Style #6912

Sold at: Justice and Limited Too stores and online at www.shopjustice.com from November 2008 through February 2010 for between $7 and $16.

Manufactured in: China

Remedy: Consumers should immediately take the recalled jewelry away from children and return it to any Justice or Limited Too store for a full refund.

Consumer Contact: For additional information, contact Tween Brands at (800) 934-4497 between 9 a.m. and 5 p.m. ET Monday through Friday, or visit the firm's web site at www.shopjustice.com

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Seattle Bike Supply Recalls Bicycles and Framesets 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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: 2010 Redline Conquest Cyclocross Bicycles and Framesets

Units: About 330

Distributor: Seattle Bike Supply, of Kent, Wash.

Hazard: The bicycle fork's legs can separate from the fork crown and cause the rider to lose control, posing a fall hazard and risk of injury.

Incidents/Injuries: The firm has received five reports of cracks near the fork's crown.

Description: This recall involves all 2010 Redline Conquest Cyclocross bicycles and framesets. The bicycles and framesets were sold in yellow and black, and have aluminum frames and aluminum forks with aluminum steering tubes. "Redline" is printed on the bicycle frame. The bicycles are equipped with a 700C wheel and frame sizes ranging from 44cm to 60 cm.

Sold at: Bicycle specialty stores nationwide between July 2009 through May 2010 for about $1,400 for the bicycle and $400 for the frameset.

Manufactured in: Taiwan

Remedy: Consumers should immediately stop using the recalled bicycles and framesets and contact their local Redline bicycle dealer to receive a free fork replacement.

Consumer Contact: For additional information, contact Redline Bicyles at (800) 283-2453 between 9:00 a.m. and 5:00 p.m. PT Monday through Friday, or visit the firm's website at www.redlinebicycles.com

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Friday, July 9, 2010

McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling 21 lots of over-the-counter medicines. The lots involved, listed below, are sold in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica. This action is a follow-up to a product recall that McNeil Consumer Healthcare originally announced on January 15, 2010, which was initiated following consumer complaints of a musty or moldy odor, which has been linked to the presence of trace amounts of a chemical called 2,4,6-tribromoanisole (TBA). The risk of serious adverse medical events is remote. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).

These lots are being added to the list of recalled products as a precautionary measure after a continuing internal review determined that some packaging materials used in the lots had been shipped and stored on the same type of wooden pallet that was tied to the presence of TBA in earlier recalled lots. All lots involved in the recall were produced before the January 15, 2010 recall, after which McNeil stopped accepting shipments of materials from its suppliers on that type of pallet.

Consumers who purchased product from the lots included in this recall should stop using the product and contact McNeil Consumer Healthcare for instructions on a refund or replacement. For these instructions, and information regarding how to return or dispose of the product, consumers should log on to the internet at www.mcneilproductrecall.com1 or call 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time). Consumers who have medical concerns or questions should contact their healthcare provider.

Any adverse reactions may also be reported to 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 website at www.fda.gov/safety/medwatch/default.htm.2

The product lot numbers for the recalled products can be found on the side of the bottle label.

FULL RECALLED PRODUCT LIST:

Product Name
Lot Number
UPC Code
BENADRYL® ALLERGY ULTRATAB™


BENADRYL® ALLERGY ULTRATAB™ TABLETS  100 count
ABA567
312547170338
BENADRYL® ALLERGY ULTRATAB™ TABLETS 100 count
ABA574
312547170338
Children’s TYLENOL® Meltaways


CHILDREN’S TYLENOL® MELTAWAYS BUBBLEGUM  30 count
ABA544
300450519306
MOTRIN® IB


MOTRIN® IB CAPLET 24 count
ACA003
300450481030
MOTRIN® IB CAPLET bonus pack 50+25 count
ACA002
300450481764
MOTRIN® IB TABLET 100 count
AFA060
300450463043
TYLENOL®, Extra Strength


TYLENOL®, Extra Strength  EZ TABLET 225 count
ASA206
300450422378
TYLENOL®, Extra Strength  EZ TABLET 50 count
ABA005
300450422507
TYLENOL®, Extra Strength  COOL CAPLET 24 count
ABA566
300450444240
TYLENOL®, Extra Strength  CAPLET bonus pack 24+12 count
ACA025
300450444318
TYLENOL®, Extra Strength  CAPLET 50 count
AFA018
300450449078
TYLENOL®, Extra Strength  CAPLET 50 count                                                    
(included in Day/Night Pack)
ABA168
300450444530
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count Lot # ABA168 & UPC  300450444530)
AEC005
300450527103
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count Lot # ABA168 & UPC  300450444530)
AFC005
300450527103
TYLENOL®, Day & Night Value Pack
(contains Extra Strength CAPLET 50 count Lot # ABA168 & UPC  300450444530)
ADC002
300450527103
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 24 count
ACA024
300450488244
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 225 count
AJA119
300450488251
TYLENOL® PM


TYLENOL® PM CAPLET 24 count
ACA005
300450482242
TYLENOL® PM CAPLET 24 count
ADA259
300450482242
TYLENOL® PM GELTAB 50 count
AFA100
300450176509
TYLENOL® PM RAPID RELEASE GELCAP 20 count
ACA004
300450244208



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Thursday, July 8, 2010

Campus Cruisers Recalls Bicycles Due to Front Fork Failure

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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of product: Eastside Fix Bicycle Forks

Units: About 100

Distributor: Campus Cruisers LLC, of Boulder, Colo.

Hazard: The bicycle's front fork can crack or break, causing a sudden loss of steering control and posing a fall hazard to bicyclists.

Incidents/Injuries: The firm has received four reports of lateral cracks beneath the front fork's crown. No injuries have been reported.

Description: This recall involves Campus Cruisers' Eastside Fix model bicycles. The single speed bicycle has an aluminum frame and fork. The bicycles were sold in royal blue with a white leather seat and white gel grips on the handlebars.

Sold at: Independent bicycle dealers nationwide from March 2010 through May 2010 for about $450.

Manufactured in: China

Remedy: Consumers should immediately stop riding bicycles with the recalled front forks. Consumers can contact their local Campus Cruisers dealer to schedule a free repair. Consumers who are not near an authorized dealer should contact Campus Cruisers for assistance.

Consumer Contact: For additional information, contact Campus Cruisers toll-free at (877) 260-2721 between 9 a.m. and 5 p.m. MT Monday through Friday or visit the firm's website at www.campuscruisers.com. Consumers can also email the firm at info@campuscruisers.com

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Wednesday, July 7, 2010

Merrick Pet Care Recalls Beef Filet Squares 10oz Bag (Item #60016 Lot # 10084TL7 Best By March 24, 2012) Because Of Possible Salmonella Health Risk

Merrick Pet Care, Inc. of Amarillo, Texas is recalling 86 cases of its 10oz “Beef Filet Squares for Dogs” pet treats (ITEM # 60016 LOT # 10084TL7 BEST BY MARCH 24, 2012) because they have the potential to be contaminated with Salmonella. Salmonella can affect animals and there is risk to humans from handling contaminated pet products. People handling the treats can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with the chews or any surfaces exposed to these products. Consumers should dispose of these products in a safe manner by securing them in a covered trash receptacle.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers immediately.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian immediately.

The Beef Filet Squares were shipped to distributors and retailers throughout the US. These individuals have been notified and have activated their recall procedures.

The treats are sold in 10oz plastic bags marked with “Lot # 10084TL7 Best By Mar 24, 2012” on the top of the bag and on a sticker applied to the bottom.

No illnesses have been reported to date. FDA collected a surveillance sample of “Merrick Beef Filet Squares for Dogs” (lot #10084TL7) which were purchased from a retail store. The sample tested positive for Salmonella.

Consumers who have purchased 10 ounce packages of “Beef Filet Squares for Dogs” are urged to return the unused portion to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-664-7387 M-F 8:00 – 5:00 CDT.

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Monday, July 5, 2010

Scope(r) Original Mint Mouthwash Recalled by Procter & Gamble Due to Failure to Meet Child-Resistant Closure Requirement

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, recently announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Scope(r) Original Mint Mouthwash, 1 Liter Size

Units: About 35,000 bottles

Manufacturer: The Procter & Gamble Co., of Cincinnati, Ohio

Hazard: The mouthwash contains ethyl alcohol and certain bottles have malfunctioning child-resistant caps and lack the statement, "This Package for Households Without Young children," as required by the Poison Prevention Packaging Act. Ethyl alcohol is toxic and can cause serious injury or death if ingested by children.

Incidents/Injuries: None reported

Description: This recall involves some bottles of Scope(r) Original Mint Mouthwash in 1 liter sizes. The recalled bottles have the number 4 on the bottom of the bottle. The bottles with the 4 on the bottom may not be child-resistant. Consumers can also attempt to twist the cap open. If the cap can be twisted off without squeezing the tabs on the cap, the package is not child-resistant.

Sold at: Drug stores, grocery stores and other retailers between January 2010 and June 2010 for about $4.

Manufactured in: United States

Remedy: Consumers should keep this product out of the reach of children. Consumers who purchased the product with the expectation that it would be in child-resistant packaging can contact Procter & Gamble for a full refund or a replacement coupon. Adult consumers can continue to use the product as directed.

Consumer Contact: For additional information, contact Procter & Gamble toll-free at (877) 340-8825 between 9 a.m. and 6 p.m. ET Monday through Friday or log on to their website at: www.scopemouthwash.com

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United Pet Group Voluntarily Expands Recall of Nutritional Supplements For Dogs to Include Additional Tablet and Powdered-Form Products for Dogs and Cats Because of Possible Salmonella Health Risk

United Pet Group, Cincinnati, Ohio is voluntarily expanding its recent recall of its Pro-Pet Adult Daily Vitamin Supplement tablets for Dogs to include additional pet nutritional supplement products for dogs and cats due to possible Salmonella contamination. The list of recalled products is provided below. The Food and Drug Administration is aware of this recall.

The recalled products are sold nationally at various retailers. The products include various United Pet Group Pro-Pet and Excel branded products for dogs and cats, and certain other private label brands of the same products. All of the affected products are in tablet and powdered form. These products are being removed from retail stores and consumers should immediately stop feeding these supplements to their pets. The affected products are those with expiration dates that include and are between "01/2013" and "06/2013." Products with expiration dates earlier than 01/2013 or later than 06/2013 are not included in this recall. The expiration date can be found imprinted vertically on the right side of the product label.

Laboratory testing has revealed that some lots of some of these products may be contaminated with Salmonella. The company is recalling the additional products out of an abundance of caution.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

People who handle these products can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with them or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with the product should contact their healthcare providers.

Consumers who have purchased the affected products are urged to contact United Pet Group or the place of purchase for further direction. Consumers may contact United Pet Group at 1-877-399-5226, Monday through Friday, from 8:30 am to 5:00 pm EST.

TABLE OF RECALLED PRODUCTS
Label Sku UPC Label Description Expiry
353 825141273447 Doctors Foster and Smith Brewers Yeast Mega-Tabs with Garlic and Essential Fatty Acids 180 Tablets EXP 01/13 thru 06/13
5619 18065056191 5619 Nature's Miracle Pet Mess Easy Clean-up Net WT 12oz EXP 01/13 thru 06/13
1152092 800443076576 Petco Breath Tabs for Dogs Liver Flavor 50 TabletsPetco Breath Tabs for Dogs Liver Flavor 50 Tablets EXP 01/13 thru 06/13
33805 825141059485 Doctors foster and Smith Dis-Taste Small Dog Tablets 250 Tablets EXP 01/13 thru 06/13
33806 825141008629 Doctors Foster and Smith Ext Strength Dis-Taste Tablets 180 Tablets EXP 01/13 thru 06/13
33807 825141063680 Doctors Foster and Smith Ext Strength Dis-Taste Tablets 500 Tablets EXP 01/13 thru 06/13
35908 825141095629 Doctors Foster and Smith Fresh Breath Tablets for Dogs 100 Tablets EXP 01/13 thru 06/13
36763 825141291250 Doctors Foster and Smith Cran Health Support Normal Urinary Tract Health 60 Tablets EXP 01/13 thru 06/13
673110 bottle
1094181 box
800443037065 Petco Ear Powder For Dogs 1oz (28g) Box Label EXP 01/13 thru 06/13
72157 825141055043 Doctors Foster and Smith Brewers Yeast Tablets for Dogs and Cats 750 Tablets EXP 01/13 thru 06/13
9305 825141003921 Doctors Foster and Smith Ear Powder Net WT 1oz (28g) EXP 01/13 thru 06/13
9306 825141005154 Doctors Foster and Smith Ear Powder Net WT 4oz (113g) EXP 01/13 thru 06/13
J707 26851007074 Excel 3 in 1 Ear Powder Ear Care Net WT 1oz(28g) EXP 01/13 thru 06/13
J7110 26851071105 Excel Glucosamine Joint Care 120 Tasty Chew Tabs EXP 01/13 thru 06/13
J7113 26851071136 Excel Glucosamine with MSM Joint Care 120 Tasty Chew Tabs EXP 01/13 thru 06/13
J720 26851007203 Excel Deter Coprophagia Treatment Behavioral Aid 60 Tasty Chew Tabs EXP 01/13 thru 06/13
J724 26851007241 Excel Deter Coprophagia Treatment Behavioral Aid 500 Tasty Chew Tabs EXP 01/13 thru 06/13
J7311 26851073116 Excel Gas Preventative Digestive Aid Digestive Care 60 Tasty Chew Tabs EXP 01/13 thru 06/13
J7315 26851073154 Excel Calm-Quil Calming Tablets Behavior Aid 60 Tasty Chew Tabs EXP 01/13 thru 06/13
J74016 26851074014 DDS Dental Breath Mints Breath Control 40 Tablets EXP 01/13 thru 06/13
K1723 26851017233 DDS Dental Breath Tabs Breath Control 200 Tablets EXP 01/13 thru 06/13
K1775 26851017752 Pro-Pet Brewers Yeast Daily Supplement 250 Chew Tablets EXP 01/13 thru 06/13
K701 26851007012 Excel Calcium Daily Supplement 125 Tasty Chew Tabs EXP 01/13 thru 06/13
K746 26851007463 Excel Calcium Daily Supplement 500 Tasty Chew tabs EXP 01/13 thru 06/13
K776/PR 26851007760 PR Excel Brewers Yeast with Garlic Skin and Coat 150 Tasty Chew Tabs EXP 01/13 thru 06/13
K777/1 26851007777 Excel Brewers Yeast with Garlic Skin and Coat Care 600 Tasty Chew Tabs EXP 01/13 thru 06/13
K778 26851007784 Excel Brewers Yeast with Garlic Skin and Coat Care 1000 Tasty Chew Tabs EXP 01/13 thru 06/13
K785 26851007852 Excel Brewers Yeast with Garlic Skin and Coat Care Mega Tabs 216 Tasty Chew Tabs EXP 01/13 thru 06/13
N1701 26851017011 Pro-Pet Senior Daily Vitamin Supplement 100 Tasty Tablets EXP 01/13 thru 06/13
N700TR 26851007005 Excel Pupply Multi Vitamin 100 Tasty Chew Tabs Time Release EXP 01/13 thru 06/13
N7301 26851073017 Excel Small Breed Multi Vitamin 45 Tasty Chew Tabs EXP 01/13 thru 06/13
N7309 26851073093 Excel Lutein Vision Maintenance Eye Care 60 Tasty Chew Tabs EXP 01/13 thru 06/13
N845TR 26851008453 Excel Adult Multi Vitamin 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78030 26851780304 Excel Advantage Adult Multi Vitamin 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78031 26851780311 Excel Advantage Puppy Multi Vitamin 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78032 26851780328 Excel Advantage Senior Multi Vitamin 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78033 26851780335 Excel Advantage Skin and Coat Essentials 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78034 26851780342 Excel Advantage Glucosamine Plus 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78035 26851780359 Excel Advantage Glucosamine Advanced Strength 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78065 26851780656 Excel Adult Multivitamin 120 Tasty Chew Tabs EXP 01/13 thru 06/13
P-78066 26851780663 Excel Senior Multi Vitamin 120 Tasty Chew Tabs EXP 01/13 thru 06/13
P-82530 26851825302 Pro-Pet Glucosamine Joint Care 60 Chew Tablets EXP 01/13 thru 06/13
P-82531 26851825319 Pro-Pet Stool-Eating Preventative(Corprophagia Treatment) 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-82534 26851825340 Pro-Pet Anti-Stress Calming Tabs 60 Chew Tablets EXP 01/13 thru 06/13
P-82562 26851825623 Pro-Pet Glucosamine Plus Joint Care 100 Chew Tablets EXP 01/13 thru 06/13
P-82618 26851826187 Pro-Pet Breath Tabs 40 Tablets EXP 01/13 thru 06/13
P-82619 26851826194 Pro-Pet Breath Mints 200 Tablets EXP 01/13 thru 06/13
P-82654 26851826545 Pro-Pet Gas Relief Digestive Aid 40 Chew Tablets EXP 01/13 thru 06/13
P-82656 26851826569 Pro-Pet Glucosamine Advanced Joint Powder Net WT 10oz(283g) EXP 01/13 thru 06/13
P-82658 26851826583 Pro-Pet Daily Vitamin Supplement Powder Net WT 10oz (283g) EXP 01/13 thru 06/13
P-83062 26851830627 Pro-Pet Puppy and Small Breed Daily Vitamin Supplement 100 Chew Tablets EXP 01/13 thru 06/13
P-83065 26851830658 Pro-Pet Glucosamine Advanced Joint Care 60 Chew Tablets EXP 01/13 thru 06/13
P-N78012 26851780120 Excel Joint Ensure Moderate Care 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-N78013 26851780137 Excel Joint Ensure Advanced Care 60 Tasty Chew Tabs EXP 01/13 thru 06/13
P-N78014
26851780144
Excel Flare-Away Joint Tabs 60 Tasty Chew Tabs EXP 01/13 thru 06/13



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