Recall Roundup: October 2010

Friday, October 29, 2010

Dollar Tree Recalls Children's Halloween Lanterns Due to Fire and Burn Hazards

Tuesday, October 26, 2010

GE Recalls Dishwashers Due to Fire 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. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product : GE Profile™ and GE Monogram® Dishwashers

Units: About 174,000

Manufacturer: GE Appliances &Lighting, of Louisville, Ky.

Hazard: Water condensation can drip onto the electronic control board, causing a short circuit and resulting in an overheated connector. This poses a fire hazard to consumers.

Incidents/Injuries: GE has received five reports of fires, four of which caused minor damage to the kitchen countertops where the dishwashers were installed and one caused minor damage to adjacent cabinets and smoke damage to the home. No injuries have been reported.

Description: This recall involves the GE Profile dishwashers manufactured between July 2002 and December 2005 and GE Monogram dishwashers manufactured between January 2004 and December 2006. They were sold in white, black, bisque, stainless steel and with custom panels. The recalled model and serial numbers listed below are located on the inside on the front left side of the dishwasher tubs.

Brand	Model Number Begins With:	Serial Number Begins With:
GE Profile	PDW9200J, PDW9280J	MF, RF, SF, TF, VF, ZF, AG, DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH, VH, ZH
	PDW9800J, PDW9880J	MF, RF, SF, TF, VF, ZF, AG, DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH
	PDW9700J	MF, RF, SF, TF, VF, ZF, AG, DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH
GE Monogram	ZBD6800K00, ZBD6800K01, ZBD6800K03, ZBD6800K10	AG, DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH, VH, ZH, AL, DL, FL, GL, HL, LL, ML, RL
	ZBD6880K00, ZBD6880K01, ZBD6880K03, ZBD6880K10	AG, DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH, VH, ZH, AL, DL, FL, GL, HL, LL, ML, RL, SL, TL, VL, ZL
	ZBD6890K00, ZBD6890K01, ZBD6890K03, ZBD6890K10	DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH, VH, ZH, AL, DL, FL, GL, HL, LL, ML, RL, SL
	ZBD0700K00, ZBD0700K01, ZBD0700K03, ZBD0700K10	VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH, VH, ZH, AL, DL, FL, GL, HL, LL, ML, RL, SL
	ZBD0710K00, ZBD0710K01, ZBD0710K03, ZBD0710K10	RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH, TH, VH, ZH, AL, DL, FL, GL, HL, LL, ML, RL, SL, TL, VL

Sold at: Retail stores nationwide, appliance dealers and authorized builder distributors from July 2003 through December 2006 for between $750 and $1,400.

Manufactured in: United States

Remedy: Consumers should immediately stop using the recalled dishwashers, disconnect the electric supply by shutting off the fuse or circuit breaker controlling it and inform all users of the dishwasher about the risk of fire. Contact GE for a free in-home repair or to receive a GE rebate of $200 for the purchase of a new GE Profile dishwasher and a GE rebate of $400 for purchase of a new GE Monogram dishwasher.

Consumer Contact: For additional information, contact GE toll-free at (877) 275-6840 from 8 a.m. to 5 p.m. ET Monday through Friday or visit the company's website at www.geappliances.com/recall.

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Monday, October 25, 2010

Working with FDA, Standard Homeopathic Company Voluntarily Recalls Hyland’s Teething Tablets to Address Manufacturing Process

Standard Homeopathic Company, in consultation with the U.S. Food and Drug Administration (FDA), is voluntarily recalling its Hyland's Teething Tablets. The company is initiating this recall in an abundance of caution due to an FDA investigation of its manufacturing facility. Hyland’s Teething Tablets are manufactured in the United States and distributed throughout North America.

The Hyland’s Teething Tablets UPC codes included in the recall are:

1. Hyland’s Teething Tablets, 125 tablets, UPC # 3 54973 75041
2. Hyland’s Teething Tablets, 250 tablets, UPC # 3 54973 75042
3. Hyland’s Teething Tablets, 125 tablets, UPC # 3 54973 75066
4. Hyland’s Teething Tablets, 50 tablets, UPC # 3 54973 75044
5. Hyland’s Teething Tablets, 145 tablets, UPC # 3 54973 75121
6. Hyland’s Teething Tablets, Clip Strip 6x125 tablets, UPC # 3 54973 35109

Adverse events have been reported but the FDA has said that a conclusive link to Teething Tablets has not been determined. The company, in working with the FDA, has identified manufacturing processes of Teething Tablets that can be improved to ensure uniformity in dosage. As a homeopathic product, Hyland’s Teething Tablets have a wide margin of safety that protects consumers from harm.

After in-depth analysis, a comprehensive review of the company’s adverse event report log, and more than 85 years of safe usage, the company is confident that Hyland’s Teething Tablets are safe for infants and toddlers.

In addition to the product recall, Standard Homeopathic Company is refining its production, packaging and testing protocols. Throughout the process, Standard Homeopathic Company will continue to closely monitor and evaluate the situation and consult with FDA.

Consumers that are concerned about the safety of the product may contact Standard Homeopathic Company for instructions on a refund or replacement product. For these instructions or information regarding how to return or dispose of the product, consumers should log on to www.hylandsteething.com/recall9 or call 1-877-496-5044 (Monday-Friday 8 a.m. to 10 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time).

"We initiated this voluntary recall to ensure our consumers know that their families' safety and health are our top priorities," said Mark Phillips, PharmD, President and Chief Pharmacist of Standard Homeopathic Company. "We are committed to maintaining and deserving the trust they have placed in Hyland's. We have worked for 107 years to build relationships with our consumers. We intend to preserve that tradition of trust."

Hyland's Teething Tablets is a homeopathic product intended to provide temporary relief of teething symptoms in children that is sold over-the-counter (OTC) in retail outlets.

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, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch10.

With over 100 years of experience in providing families with access to safe, natural, reliable medicines, Standard Homeopathic Company and its division, Hyland’s, Inc., have many symptom fighting products consumers have come to trust. For more information on their line of products, visit www.hylands.com11 or www.facebook.com/Hylands.Health.

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Nestlé® USA Issues Allergen Alert on Single Production Code of Nestlé® Raisinets® Fun Size Bags

Nestlé USA's Confections &Snacks Division is initiating a voluntary recall of Nestlé® RAISINETS® Fun Size Bags (10oz) with a production code of 02015748/UPC number 2800010255, which may contain undeclared peanuts. People who have allergies or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. Nestlé is taking this action out of an abundance of caution.

Nestlé® RAISINETS® Fun Size Bags (10oz) with a production code of 02015748 were distributed only in the U.S. to Target, Shop Rite and Don Quixote retail stores. Three complaints have been received to date. While this product is labeled with a precautionary statement "made on equipment that also processes peanuts," the product should not, but may contain some peanuts that are not declared on the label.

Providing safe, high quality products to our consumers is our number one priority. We have advised the U.S. Food and Drug Administration and will cooperate fully in their investigation. The only product involved is Nestlé® RAISINETS® Fun Size Bags (10oz) distributed in the U.S. with a production code of 02015748/UPC number 2800010255. No other Nestlé products are impacted.

Consumers who are allergic to peanuts and who have purchased the recalled products are advised by Nestlé not to consume them. Instead, Nestlé asks these consumers to contact Nestlé Consumer Services directly at 1-800-478-5670 for a full refund and discard any remaining packages. Consumers should not return Nestlé® RAISINETS® Fun Size Bags (10oz) with a production code of 02015748/UPC number 2800010255 to retailers. Operators are available between 8 a.m. and 8 p.m. EST and after hours for emergencies. Those with questions should contact Nestlé Consumer Services at 1-800-478-5670 or via email at nestlecandy@casupport.com. Nestlé apologizes for any inconvenience experienced by our valued consumers and retail customers.

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Friday, October 22, 2010

Claire-Sprayway Recalls Fabric Protector Due to Respiratory Hazard

Frigidaire and Electrolux ICON Electric Smoothtop Cooktops and Slide-In Ranges Recalled Due to Fire Hazard

Thursday, October 21, 2010

Graco Recalls Quattro(tm) and MetroLite(tm) Strollers Due to Risk of Entrapment and Strangulation

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.

The U.S. Consumer Product Safety Commission (CPSC), in cooperation with Graco Children's Products Inc., of Atlanta, Ga., is announcing the recall of about 2 million Graco strollers due to risk of entrapment and strangulation. CPSC and Graco have received four reports of infant strangulations that occurred in these strollers between 2003 and 2005. In addition, CPSC is aware of five reports of infants becoming entrapped, resulting in cuts and bruises, and one report of an infant having difficulty breathing.

Entrapment and strangulation can occur, especially to infants younger than 12 months of age, when a child is not harnessed. An infant can pass through the opening between the stroller tray and seat bottom, but his/her head and neck can become entrapped by the tray. Infants who become entrapped at the neck are at risk of strangulation.

The recall involves older versions of the Graco Quattro Tour(tm) and MetroLite(tm) strollers and travel systems manufactured prior to the existence of the January 2008 voluntary industry standard which addresses the height of the opening between the stroller's tray and the seat bottom. This voluntary standard requires larger stroller openings that prevent infant entrapment and strangulation hazards.

This recall involves Graco Quattro Tour(tm) strollers and travel systems manufactured prior to November 2006 and MetroLite(tm) strollers and travel systems manufactured prior to July 2007. The strollers and travel systems were distributed between November 2000 and December 2007. The model numbers are printed on a label at the lower portion of the rear frame, just above the rear wheels or underneath the stroller. The name "Graco" appears on a label on the stroller tray and the headrest. Models included in the recall are:

Quattro Stroller, $100-$190, Distributed Between Nov 2002 - Dec 2007: 35735, 35759, 7111ASB, 7111BKW, 7111CLN, 7111CUN, 7111DIA, 7111HEA, 7111HIG, 7111LAG, 7111KSH, 7112CNP, 7112MTR, 7113CJR, 7113CMR, 7113COT, 7119GGG, 7119WSR, 7121MAY, 7125QST, 7126RNS, 7127LEG, 7132RXY, 7134SMB, 7138RNS

Quattro Stroller Travel System, $200-$250, Distributed Between Oct 2002 - Oct 2007: 35760, 7411ATR, 7411BGN, 7411BGN2, 7411BLB, 7411KBK, 7411KBK2, 7411LV, 7411MCH, 7411MCH2, 7411MLY, 7411MLY2, 7419LIM, 7419LIM2, 7419OWD2, 7B00BDA, 7B00DRB, 7B00KAS, 7B01MNS, 7B03CST2, 7B03LTC2, 7B03TFE2

MetroLite Stroller, $90-$190, Distributed Between Nov 2000 - Dec 2007: 1104, 1240, 6110DW, 6110F3, 6110S7, 6110TS7, 6111FKB, 6111VIN, 6113SCR, 6114HAV, 6114JAM, 6114LAG, 6114NGS, 6116NRF, 6120SHL, 6121CJG, 6121CNP, 6121GGG, 6121MTR, 6123EME, 6124LRD, 6125SMB, 6J01DAI, 6J01HRL, 6J03RIT, 6J04JEN, 6J05MIN

MetroLite Travel System, $190-$250, Distributed Between Dec 2000 - June 2005: 1070, 7000KSB, 7308DEL, 7308DEL2, 7308DEL4, 7308TYR, 7308TYR2, 7406PLT, 7408MRT, 7409GRG, 7410CON, 7413CML, 7413MRN, C7413CML

NOTE: Quattro and MetroLite strollers ending with the number 3 are NOT affected by this recall.

The strollers were sold at AAFES, Babies R Us, Burlington Coat Factory, Fred Meyer, Kmart, Meijers, Navy Exchange, Sears, Target, Walmart and other stores nationwide between November 2000 and December 2007 for between $90 and $190 for the strollers, and between $190 and $250 for travel systems.

The strollers were manufactured in China.

Consumers should immediately stop using the recalled strollers and contact Graco for a free repair kit. To order a repair kit, contact Graco toll-free at (877) 828-4046 anytime, or visit the firm's website at www.gracobaby.com. Consumers can continue use of the stroller as a "travel system." When the stroller is used with the infant car seat, the entrapment and strangulation hazards posed by the space gap are not present.

For additional information, consumers can contact Graco at (800) 345-4109 between 8 a.m. and 5 p.m. ET Monday through Friday.

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Wednesday, October 20, 2010

Infant's Overalls Recalled by Lollytogs Due to Choking 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 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: Infant's Overalls

Units: About 8,300 units in the United States and 2,000 in Canada

Distributor: Lollytogs Ltd., of New York, N.Y.

Hazard: The overalls have snaps that could come loose and pose a choking hazard to young children.

Incidents/Injuries: None reported.

Description: This recall involves infants' Carhartt(r) overalls with style numbers GG8500 (100% cotton canvas) and GG8501 (100% cotton knit). The overalls were sold in brown or red in infant sizes 3, 6, 9, 12, 18 and 24 months. The Carhartt logo is sewn on the front of the garment and the style numbers can be found on the sewn-in label hanging from the sleeve.

Sold at: Retailers nationwide from February 2010 through July 2010 for about $25.

Manufactured in: India

Remedy: Consumers should immediately take the overalls away from children and return them to the place of purchase for a full refund or store credit.

Consumer Contact: For additional information, contact Lollytogs at (800) 637-9035 between 9 a.m. and 5 p.m. ET Monday through Friday or visit the firm's website at www.ltapparel.com

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Dollar Tree Recalls Children's Projector Flashlights Due to Fire and Burn Hazards

Tuesday, October 19, 2010

McNeil Consumer Healthcare Announces Voluntary Recall of One Product Lot of TYLENOL® 8 Hour Caplets 50 Count Sold in The United States and Puerto Rico

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling one product lot of TYLENOL® 8 Hour caplets 50 count bottles to the retail level. McNeil is taking this action following a small number of complaints of a musty or moldy odor. The uncharacteristic odor is thought to be caused by the presence of trace amounts of a chemical called 2,4,6-tribromoanisole. This voluntary action is being taken as a precaution and the risk of adverse medical events is remote. To date, observed events reported to McNeil for this lot were temporary and non-serious.

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

FULL RECALLED PRODUCT LIST:

Product Name Lot Number UPC Code

Tylenol® 8 Hour Caplet 50 count BCM155 3 0045-0297-51 8

Consumers who purchased product from the lot included in this recall should stop using the product and contact McNeil Consumer Healthcare, either at www.tylenol.com9 or by calling 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) for instructions about receiving a refund or product coupon. Consumers who have medical concerns or questions should contact their healthcare provider.

Any adverse reactions may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

* Online:www.fda.gov/medwatch/report.htm10
* Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm11. Mail to address on the pre-addressed form.
* Fax: 1-800-FDA-0178

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

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Bathtub Toys Recalled by Munchkin Due to Risk of Injury

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: Bathtub Subs

Units: About 34,000 units

Importer: Munchkin Inc, of North Hills, Calif.

Hazard: The intake valve on the bottom of the submarine toy can suck up loose skin, posing laceration hazard to children.

Incidents/Injuries: CPSC and the company are aware of 19 incidents of lacerations to boys' genital area. One of the incidents required medical attention.

Description: This recall involves battery-operated bathtub submarine toys. The toy is yellow, has a smiling face, turquoise windows, an orange propeller and an orange periscope that turns the toy on and off. The intake valve has a water pump that sucks in water to propel the submarine. The toy is intended for use by children during bath time.

Sold at: Mass merchandise retail stores nationwide and children's stores nationwide from November 2009 through September 2010 for about $7.

Manufactured in: China

Remedy: Consumers should immediately take the recalled toy away from children and contact Munchkin for instructions on how to return the product for a free replacement toy.

Consumer Contact: For additional information, contact Munchkin at (877) 242-3134 anytime or visit the company's website at http://www.munchkin.com/

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Monday, October 18, 2010

The Pictsweet Company Issues Allergy Alert On Undeclared Milk In 32 Ounce Clear Bag Breaded Okra

The Pictsweet Company of Bells, TN is recalling specific lots of Pictsweet 32 ounce Clear Bag Breaded Okra because they contain undeclared milk product. People who have an allergy or severe sensitivity to milk may run the risk of serious allergic reaction if they consume this product.

This recall affects only Pictsweet 32 ounce Clear Bag Breaded Okra with production codes beginning with the following five digits: 1400B, 1550B, 1660B, 1730B, 1870B, 2030B, 2350B, 2500B and was distributed to retailers in the Southeast United States.

The company initiated this recall after it was discovered that product containing milk was distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicated the problem was caused by a packaging redesign that included the incorrect ingredient statement.

No illnesses or allergic reactions have been reported to date.

Consumers who have an allergy or severe sensitivity to milk products and have purchased Pictsweet 32 ounce Clear Bag Breaded Okra with one of the codes listed above are urged to contact the company at 1-800-367-7412, extension 417 from 9am to 5pm Central Daylight Time, Monday – Friday or return the product to the place of purchase for a full refund.

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The Pictsweet Company Announces a Voluntary Recall of Frozen Green Peas Due to Possible Health Risk

The Pictsweet Company of Bells, TN today announced a voluntary recall of certain codes of store brand products containing frozen Green Peas after the company learned that some of the packages may contain glass fragments, which may cause injury if ingested.

Products subject to this recall were distributed only to Kroger stores in the Southeast United States and Walmart stores throughout the United States and include the following items:

* Kroger 12 ounce Green Peas (UPC 11110 89736)
Production Codes of 1440BU, 1440BV, 1440BW, and 1600BD
* Kroger 12 ounce Peas and Carrots (UPC 11110 89741)
Production Codes of 1960BD and 1960BE
* Great Value 12 ounce Steamable Sweet Peas (UPC 78742 08369)
Best by Dates of July 20, 2012; July 21, 2012
* Great Value 12 ounce Steamable Mixed Vegetables (UPC 78742 08026)
Best by Date of July 15, 2012

No injuries have been reported to date. While no injuries have been reported, Pictsweet is advising the public that product from these packages indicated above should not be consumed. Consumers who have purchased the above product should return them to the place of purchase for a full refund.

Consumers with questions may contact The Pictsweet Company at 1-800-367-7412, extension 417 toll-free from 9:00 a.m. to 5:00 p.m. Central Daylight Time, Monday through Friday.

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Thursday, October 14, 2010

The Pictsweet Company Issues Allergy Alert on Undeclared Milk in 32 Ounce Clear Bag Breaded Okra

/PRNewswire/ -- The Pictsweet Company of Bells, TN is recalling specific lots of Pictsweet 32 ounce Clear Bag Breaded Okra because they contain undeclared milk product. People who have an allergy or severe sensitivity to milk may run the risk of serious allergic reaction if they consume this product.

This recall affects only Pictsweet 32 ounce Clear Bag Breaded Okra with production codes beginning with the following five digits: 1400B, 1550B, 1660B, 1730B, 1870B, 2030B, 2350B, 2500B and was distributed to retailers in the Southeast United States.

The company initiated this recall after it was discovered that product containing milk was distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicated the problem was caused by a packaging redesign that included the incorrect ingredient statement.

No illnesses or allergic reactions have been reported to date.

Consumers who have an allergy or severe sensitivity to milk products and have purchased Pictsweet 32 ounce Clear Bag Breaded Okra with one of the codes listed above are urged to contact the company at 1-800-367-7412, extension 417 from 9am to 5pm Central Daylight Time, Monday – Friday or return the product to the place of purchase for a full refund.

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Ryobi Recalls Cordless Drills Due to Fire Hazard

Iron Lover's Bench Sold Exclusively at Ross Stores Recalled Due to Fall Hazard

Monday, October 11, 2010

Lipitor Recall Information

Pfizer recalled specific bottles of LIPITOR (40 mg only) due to a small number of reports of an uncharacteristic odor related to the bottles in which LIPITOR is packaged. A medical assessment has determined that the odor is not likely to cause adverse health consequences in patients taking LIPITOR. There is no need to take any action if you take LIPITOR; please continue to take your medication as prescribed by your doctor. However, if you take LIPITOR 40 mg and experience an uncharacteristic odor associated with your medication, please return the tablets to your pharmacist.

Pfizer is committed to the safety of patients who take our medicines. Pfizer is working closely with the bottle supplier to determine the cause of the odor problem and to rapidly address it. Pfizer responded rapidly to ensure LIPITOR continues to meet the company’s high quality standards. We will continue to actively monitor the situation and take any action necessary to ensure patient safety and maintain the quality of our products.

If you have any questions about LIPITOR, please contact your doctor or your pharmacist or call 1-888-LIPITOR.

Common Questions

Why was LIPITOR recalled?
Pfizer has recalled specific “lots” or batches of LIPITOR (40 mg only) due to a small number of reports of an uncharacteristic odor related to the bottles in which the product is packaged. Pfizer is working closely with the bottle supplier to determine the cause of the odor problem and to rapidly address it.

Where can people go for more information about the recall?
If you have any questions about the recall please call 1-888-LIPITOR. If you have specific questions about your medication, you may also call your doctor or pharmacist.

I take LIPITOR. What should I do?
Pfizer recalled only specific bottles of LIPITOR 40 mg due to a small number of reports of an uncharacteristic odor and a medical assessment has determined that the odor is not likely to cause adverse health consequences in patients taking LIPITOR. Medication should always be taken as prescribed by a doctor. If you take LIPITOR 40 mg and experience an uncharacteristic odor associated with your medication, please return the tablets to your pharmacist.

If you take LIPITOR and experience an odd smell or odor, what should you do?
Pfizer recalled only specific bottles of LIPITOR 40 mg due to a small number of reports of an uncharacteristic odor and a medical assessment has determined that the odor is not likely to cause adverse health consequences in patients taking LIPITOR. If you take LIPITOR 40 mg and experience an uncharacteristic odor associated with your medication, please return the tablets to your pharmacist. If you have any concerns, call your doctor or pharmacist or call 1-888-LIPITOR if you need any further information.

Is it still safe to take LIPITOR?
Pfizer has recalled only specific bottles of LIPITOR 40 mg due to a small number of reports of an uncharacteristic odor related to the bottles in which LIPITOR is packaged. A medical assessment has determined the odor is not likely to cause adverse health consequences in patients taking LIPITOR. Pfizer remains confident in the safety and efficacy of LIPITOR.

Will there be a LIPITOR 40 mg shortage as a result of the recall?
Pfizer has taken a number of steps to ensure that there is no shortage of LIPITOR 40 mg as a result of this recall.

Can I get a refund if I take LIPITOR 40 mg?
Pfizer has recalled only specific bottles of LIPITOR 40 mg. Please speak to your pharmacist about refund policies. Pfizer is not offering a refund.

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Blue Buffalo Company, Ltd. Recalls Limited Production Code Dates of Dry Dog Food Because of Possible Excess Vitamin D

Blue Buffalo Company, Ltd., recalls certain dry dog food because of possible excess Vitamin D that can affect the health of some dogs. The Blue Buffalo Company, Ltd., is recalling certain packages of its Wilderness Chicken, Basics Salmon and Large Breed Adult Chicken dry dog foods sold under thc "BLUE" brand which have the potential to contain excessive levels of Vitamin D.

While Vitamin D is a beneficial component of these foods, the Company believes that these products may have levels of Vitamin D that are beyond the formula specifications, and has therefore chosen to withdraw them.

Dogs reacting to the higher levels of Vitamin D may show signs of lethargy or exhibit unusually frequent water consumption and urination. If your pet has consumed the recalled products and has these symptoms, please contact your veterinarian.

The affected productions of Blue Wilderness Chicken, Basics Salmon and Large Breed Adult Chicken dry dog foods were distributed nationwide through pet specialty stores.

Only these production runs of the products are involved in this recall:

Blue Wilderness Chicken Flavor dry dog food	4.5 1b	"Best If Used By JUL2611Z" "Best If Used By JUL2711Z" & "Best If Used By JUL2811Z"
Blue Wilderness Chicken Flavor dry dog food	11 lb	"Best If Used By JUL1211B"
Blue Wilderness Chicken Flavor dry dog food	24 1b	"Best If Used By JUL1211B" & "Best If Used By JUL1311B"
Blue Basics Limited Ingredient Formula Salmon and Potato Recipe dry dog food	11 lb	"Best If Used By AUG2111B" & "Best If Used By AUG2211B"
Blue Basics Limited Ingredient Formula Salmon and Potato Recipe dry dog food	24 lb	"Best If Used By AUG2111B" "Best If Used By SEP2311P" & "Best If Used By OCT2611P"
Blue Life Protection Formula Natural Chicken & Brown Rice Recipe Large Breed Adult dog food	30 lb	"Best If Used By SEP2211P" "Best If Used By SEP2311P" & "Best If Used By OCT2611P"

No other BLUE dry or can pet foods are involved in this recall, and only the specific code dates of these products are involved.

To date there have been 36 cases nationwide of dogs reported with symptoms consistent with elevated Vitamin D in their systems while feeding on these specific productions of the products. In all cases the symptoms have subsided upon discontinuing feeding these products, with no apparent long term health consequences.

Blue Buffalo learned of this potential eondition in its products when it received reports of dogs diagnosed with high Vitamin D levels while feeding on the products from these specifie production runs. On further investigation it was learned that a sequencing error had occurred at the supplier of the dry ingredients for these products. Immediately before producing the ingredients for these specific production runs, the supplier had run a product for another customer that contained a more potent form of Vitamin D used in chicken feeds. It is now believed that there was some level of carry over of this Vitamin D product into the ingredients for the specific manufacturing runs of the BLUE products, thereby increasing the Vitamin D activity to unacceptable levels in the Blue ingredients.

Consumers who have purchased any of the products being recalled are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-877-523-9114 from 8 AM to 8 PM Eastern Time or visit the Company web site at www.bluebuffalo.com/news9 for more information.

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Friday, October 8, 2010

Castalon Frying Pans Recalled By Tabletops Unlimited Due to Burn Hazard

Gaspari Nutrition Nutrition Issues a Voluntary Nationwide Recall of Novedex XT, a Product Marketed as a Dietary Supplement Containing ATD

Gaspari Nutrition Incorproated, 575 Prospect Street - Suite 230, Lakewood, NJ, announced today that it is conducting a voluntary nationwide recall of all Lot Codes of the company's dietary supplement product sold under the name Novedex XT, which was marketed "for increasing natural testosterone production" and contains 3,17-keto-etiocholetriene, also known as ATD, an anti-aromatase. Gaspari Nutrition is conducting this consumer level recall after being informed by representatives of the Food and Drug Administration (FDA) that 3,17-keto-etiocholetriene does not meet the definition of a dietary ingredient and therefore the product is in violation of provisions of the Federal Food, Drug, and Cosmetic Act.

Potential adverse events associated with the use of anti-aromatases could include the following: decreased rate of bone maturation and growth, decreased sperm production, infertility, aggressive behavior, adrenal insufficiency, kidney failure, and liver dysfunction. Consumers with liver, kidney, adrenal, or prostate abnormalities are at higher risk for developing adverse events. Gaspari has received no serious adverse events in over five years of marketing Novadex XT.

Novedex XT had been sold internationally and domestically, to distributors, wholesalers, retail stores and direct to consumers, but was discontinued by Gaspari Nutrition for domestic sales on October 4th 2010. The product was sold in blue bottles with a black cap, containing sixty (60) capsules.

Consumers who have Novedex XT in their possession should stop using it immediately. If consumers experience any adverse side effects due to consumption of this product, they should immediately contact a physician. Adverse reactions or quality problems experienced with the use of this product may be reported to Gaspari Nutrition and to the FDA's MedWatch Adverse Event Reporting program online, by regular mail, or by fax:

* Online: www.fda.gov/MedWatch/report.htm

* Regular Mail: use postage-paid, preaddressed Form FDA 3500 available at www.fda.gov/MedWatch/getforms.htm

* Fax: 1-800-FDA-0178.

The Company is advising consumers who have Novedex XT to return any unused portion to the retail location from which it was purchased or if purchased directly from Gaspari Nutrition to return any unused portion to: Gaspari Nutrition Incorporated, 575 Prospect Street - Suite 230, Lakewood, NJ 08701; Attention: Novedex XT Recall. Consumers with questions regarding this recall can contact the company at 1-732-364-3777 Monday through Friday 9 AM to 5 PM, PST. Consumers who have purchased this product and have medical concerns should consult with their health care providers.

This recall is being conducted in cooperation with the U.S. Food and Drug Administration (FDA).

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Thursday, October 7, 2010

Bravo Sports Recalls Trampolines Due to Fall Hazard

Tike Tech Recalls Jogging Strollers Due to Strangulation Hazard

Alexander Designs' Brand Drop-Side Cribs Sold Exclusively at JCPenney Recalled for Repair Due to Entrapment, Suffocation and Fall Hazards

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

Name of product: Alexander Designs Ltd. brand drop-side cribs

Units: About 11,400

Manufacturer: Jardine Enterprises Ltd., of Taipei, Taiwan

Distributor: J.C. Penney, of Plano, Texas

Hazard: The drop-side rail hardware on the cribs can break or fail, allowing the drop side to detach from the crib. When the drop side detaches, a hazardous gap is created between the drop-side rail and the crib mattress in which infants and toddlers can become wedged or entrapped, posing risks of suffocation and strangulation. In addition, children can fall out of the crib when the drop-side rail falls unexpectedly or detaches from the crib. Drop-side rail failures also can occur due to incorrect assembly or with age-related wear and tear. Other models of Jardine drop-side cribs were recalled for repair on June 24, 2010. (http://www.cpsc.gov/cpscpub/prerel/prhtml10/10275.html).

Incidents/Injuries: CPSC has received two reports of incidents involving drop-side malfunctions on Alexander Designs drop-side cribs. In one incident, which involved a crib that had been misassembled, the plastic hardware broke and the drop-side rail fell unexpectedly. In a second incident, a hardware failure caused the drop-side rail to detach from the crib. No injuries were reported.

Description: This recall involves full-size cribs sold under the Alexander Designs brand name. "Alexander Designs Ltd." and the JCPenney catalog/item number are printed on a label on the crib's headboard. The following models are included:

Model Name    JCPenney Item Number(s)                     Color

Alexander 3-in-1 Crib              343-8359                                    honey pine
                                                  343-8359                                    white

Alexander Classic Crib             343-8180                                   cherry
                                                   343-8180                                  honey pine
                                                  343-8180                                   white

Alexander Sleigh Crib              343-8802                                   cherry
                                                  343-8802                                   white

Sold through: JCPenney printed catalogs and online at JCPenney.com from March 2003 through April 2007 for about $200.

Manufactured in: China

Remedy: Consumers should immediately stop using the cribs and obtain a free repair kit that will immobilize the drop-side rail. In the meantime, parents are urged to find an alternate, safe sleeping environment for the child, such as a bassinet, play yard or toddler bed depending on the child's age.

Consumer Contact: For additional information, contact Jardine at (800) 295-1980
anytime or visit the firm's website at http://www.jdservice.biz/jcp-safety-notice.

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Saturday, October 2, 2010

Rising Dough Bakery Issues Allergy Alert on Undeclared Walnuts in the Rising Dough Brand Individual Wrapped Cranberry Muffins

Rising Dough Bakery of Sacramento, California is voluntarily recalling all Rising Dough Brand Individual Wrapped Cranberry Muffins, because it contains undeclared Walnuts. People who have an allergy or severe sensitivity to Walnuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The Cranberry Muffins were distributed nationwide and sold in retail stores.

The product is a 4 oz. Individually Wrapped Muffin topped with Streusel Crumbs. The product is incorrectly labeled on the bottom and doesn't identify Walnuts in the Allergen list. The UPC on this label is 0 48055 41359 8.

The recall was initiated after it was discovered that product containing Walnuts was distributed in packaging that did not reveal the presence of Walnuts. Subsequent investigation indicates the problem was caused by an error in proofing of the label.

Consumers who have purchased the Rising Dough Bakery Cranberry Muffin are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-877-349-8900 (6-2:30 Pacific Time)

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Friday, October 1, 2010

Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen

Hostess Brands, Inc. of Irving, Texas, is voluntarily recalling Chocolate Chip Mini Muffins multi-packs sold in retail stores throughout the United States with the knowledge of the FDA. Some of these multi-packs may contain muffins with undeclared walnuts, which is an allergen. People who have an allergy or severe sensitivity to walnuts run the risk of serious illness or life-threatening allergic reaction if they consume these products.

The Product being recalled is:

Hostess® Mini Muffins (Chocolate Chip variety)
4 Packs of 5 muffins each
Net Wt 8 oz. (227 g)
UPC 45000-60703
Stamped code of "Best By: OCT 31 $7.98/lb $3.99" printed below will be
"62 259" followed by a capital letter, a time stamp and then "1029"

To date, no incidents of illness have been reported. People who do not have walnut allergies can eat the product without concern. The packaging does contain an allergen advisory statement: "May contain walnuts."

The recall was initiated after it was discovered that during manufacturing some Banana Nut Mini Muffins were inadvertently inserted into the Chocolate Chip Mini Muffin packaging. Normally, Chocolate Chip Mini Muffins do not contain walnuts. Subsequent investigation indicates the problem was caused by operator error in the packaging process.

This error was limited to one day’s production, and no other HOSTESS® products are part of this recall.

Consumers who purchased these Mini Muffins who wish to return them should return them to the retailer for a refund or contact Hostess Brands' Consumer Affairs Office at 1-800-483-7253 (Monday –Friday 8:30 a.m. to 4:30 p.m. CST) for a replacement coupon.

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