MomToEliEm
Moderator
Here is a list of new product recalls issued this week: 03/25/11-04/01/11
Please note this list includes most recalls from CPSC, USDA, FDA, NHTSA (carseats and tires only) and boat recalls from the Coast Guard. I do not include vehicle recalls or USDA/FDA recalls related to undeclared allergins. To view all the recalls including those allergin related recalls, you can go to: http://www.recalls.gov/recent.html to see a full listing from each agency.
Exmark Recalls Pioneer S-Series Mowers Due to Crash Hazard. Sold by: Exmark dealers nationwide from February 11, 2011 to March 10, 2011 for $6,881 to $7,658.
http://www.cpsc.gov/cpscpub/prerel/prhtml11/11730.html
Toro Z Master ZRT Mowers Recalled by The Toro Company Due to Injury Hazard. Sold at: Toro dealers in the U.S. and Canada from September 2005 through January 2011 for prices ranging from $13,000 to 17,000.
http://www.cpsc.gov/cpscpub/prerel/prhtml11/11731.html
Louie Foods International of Fresno, California, is voluntarily recalling all Louie’s brand sprouts with a “Use By” date on or before 4/14/11, because they may be contaminated with Salmonella. Products were sold to distributors located in the Central Valley and along the Coast of California.
http://www.fda.gov/Safety/Recalls/ucm249283.htm
Thomas Produce of Boca Raton, FL, is recalling 320 boxes of Jalapeno Peppers because they have the potential to be contaminated with Salmonella. The recalled Jalapeno Peppers were sold to distributors in Florida, New York, North Carolina, New Jersey, Minnesota, and Pennsylvania from 2/15/2011 to 2/18/2011.
http://www.fda.gov/Safety/Recalls/ucm249201.htm
Arko Foods International of Los Angeles, CA is recalling Angelina Brand Smoked Roundscad, 8oz packs, because it has the potential to be contaminated with Clostridium botulinum. Angelina Brand Smoked Roundscad was distributed in California, Nevada, Arizona, Washington, New York, Texas, Maryland, and Florida through retail stores, supermarkets, and wholesale distributors.
http://www.fda.gov/Safety/Recalls/ucm249386.htm
Frankly Fresh, Inc. of Carson, CA. is voluntarily recalling its seafood salad line of products, because it has the potential to be contaminated with Listeria monocytogenes. Product was distributed in the California and Nevada Areas through retail supermarket stores. Products are packed under the Frankly Fresh label in a variety of sizes in plastic containers with safety seals on.
http://www.fda.gov/Safety/Recalls/ucm249270.htm
The Smokehouse LLC of Mamaroneck, New York, is conducting a voluntary recall of PORTIER FINE FOODS Norwegian Smoked Salmon of various size packages including 4 oz., 8 oz., 16 oz. and random weight sizes, Batch Code 066 only, due to potential contamination with Listeria monocytogenes. PORTIER FINE FOODS Norwegian Smoked Salmon with code 066 was distributed and sold on March 7, 2011 to retailers in NY, NJ, CT.
http://www.fda.gov/Safety/Recalls/ucm249131.htm
Nutrition Express of Torrance, CA is voluntarily recalling specific products containing whey protein isolate sourced from one supplier because they have the potential to be contaminated with Salmonella. About 450 bottles of powdered protein were sold at two retail health food stores only (Lindberg Nutrition located in Torrance and Manhattan Beach), both in Los Angeles County, California. The only other sales channel was a direct-to-consumer channel from Nutrition Express.
http://www.fda.gov/Safety/Recalls/ucm248977.htm
Circle City Marketing and Distributing, doing business as Candy Dynamics, Indianapolis, IN, is issuing a voluntary recall of Toxic Waste® Short Circuits™ Bubble Gum, 3.2 oz (90 g) size, Lot #15070SC12 due to elevated levels of lead (0.189 parts per million; the FDA tolerance is 0.1 ppm) that potentially could cause health problems, particularly for infants, small children, and pregnant women. The recalled Short Circuits™ Bubble Gum product was distributed nationwide in retail stores and through mail orders.
http://www.fda.gov/Safety/Recalls/ucm248548.htm
NAC Foods Corporation of Palisades Park, New Jersey is announcing a voluntary recall of the Mi Pepito Arnica Flower and Stem Arnica due to inaccurate usage information on the product label. The current label states ‘Use to enhance the flavor of your favorite dish.’ The label should have stated: ‘Recommended for external use only.’ The product was distributed to retail outlets in Rhode Island, Connecticut, Pennsylvania, New York and New Jersey.
http://www.fda.gov/Safety/Recalls/ucm248703.htm
APP Pharmaceuticals, Inc., (APP) announced today that it has issued a voluntary recall of five lots of Irinotecan Hydrochloride Injection, which is used for recurrent or progressive metastatic colorectal cancer. decided to take this action due to an atypical trend in customer complaints associated with lot 870DE00301.
http://www.fda.gov/Safety/Recalls/ucm248576.htm
USA Far Ocean Group Inc., 1609 W. Valley Blvd., #338, Alhambra, CA 91803, announced today that it is conducting a voluntary nationwide recall of the Company's two supplement products sold under the names X-Hero and Male Enhancer. The Company has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of X-Hero sample found the product contains sulfosildenafil. These two products have been distributed nationwide via retail stores, internet sales and mail order.
http://www.fda.gov/Safety/Recalls/ucm248718.htm
Greenstone LLC announced today that it is voluntarily conducting a recall, to the patient level, of medicines with lot number FI0510058-A on the label. This includes Citalopram 10mg Tablets (100-count bottle) and Finasteride 5mg Tablets (90-count bottle), both distributed in the U.S. market. The recall is due to the possibility that incorrect labels have been placed on the bottles by a third-party manufacturer.
http://www.fda.gov/Safety/Recalls/ucm248552.htm
If you missed last week's recall listing, here is the link to it:
http://www.car-seat.org/showthread.php?t=164785
Please note this list includes most recalls from CPSC, USDA, FDA, NHTSA (carseats and tires only) and boat recalls from the Coast Guard. I do not include vehicle recalls or USDA/FDA recalls related to undeclared allergins. To view all the recalls including those allergin related recalls, you can go to: http://www.recalls.gov/recent.html to see a full listing from each agency.
Exmark Recalls Pioneer S-Series Mowers Due to Crash Hazard. Sold by: Exmark dealers nationwide from February 11, 2011 to March 10, 2011 for $6,881 to $7,658.
http://www.cpsc.gov/cpscpub/prerel/prhtml11/11730.html
Toro Z Master ZRT Mowers Recalled by The Toro Company Due to Injury Hazard. Sold at: Toro dealers in the U.S. and Canada from September 2005 through January 2011 for prices ranging from $13,000 to 17,000.
http://www.cpsc.gov/cpscpub/prerel/prhtml11/11731.html
Louie Foods International of Fresno, California, is voluntarily recalling all Louie’s brand sprouts with a “Use By” date on or before 4/14/11, because they may be contaminated with Salmonella. Products were sold to distributors located in the Central Valley and along the Coast of California.
http://www.fda.gov/Safety/Recalls/ucm249283.htm
Thomas Produce of Boca Raton, FL, is recalling 320 boxes of Jalapeno Peppers because they have the potential to be contaminated with Salmonella. The recalled Jalapeno Peppers were sold to distributors in Florida, New York, North Carolina, New Jersey, Minnesota, and Pennsylvania from 2/15/2011 to 2/18/2011.
http://www.fda.gov/Safety/Recalls/ucm249201.htm
Arko Foods International of Los Angeles, CA is recalling Angelina Brand Smoked Roundscad, 8oz packs, because it has the potential to be contaminated with Clostridium botulinum. Angelina Brand Smoked Roundscad was distributed in California, Nevada, Arizona, Washington, New York, Texas, Maryland, and Florida through retail stores, supermarkets, and wholesale distributors.
http://www.fda.gov/Safety/Recalls/ucm249386.htm
Frankly Fresh, Inc. of Carson, CA. is voluntarily recalling its seafood salad line of products, because it has the potential to be contaminated with Listeria monocytogenes. Product was distributed in the California and Nevada Areas through retail supermarket stores. Products are packed under the Frankly Fresh label in a variety of sizes in plastic containers with safety seals on.
http://www.fda.gov/Safety/Recalls/ucm249270.htm
The Smokehouse LLC of Mamaroneck, New York, is conducting a voluntary recall of PORTIER FINE FOODS Norwegian Smoked Salmon of various size packages including 4 oz., 8 oz., 16 oz. and random weight sizes, Batch Code 066 only, due to potential contamination with Listeria monocytogenes. PORTIER FINE FOODS Norwegian Smoked Salmon with code 066 was distributed and sold on March 7, 2011 to retailers in NY, NJ, CT.
http://www.fda.gov/Safety/Recalls/ucm249131.htm
Nutrition Express of Torrance, CA is voluntarily recalling specific products containing whey protein isolate sourced from one supplier because they have the potential to be contaminated with Salmonella. About 450 bottles of powdered protein were sold at two retail health food stores only (Lindberg Nutrition located in Torrance and Manhattan Beach), both in Los Angeles County, California. The only other sales channel was a direct-to-consumer channel from Nutrition Express.
http://www.fda.gov/Safety/Recalls/ucm248977.htm
Circle City Marketing and Distributing, doing business as Candy Dynamics, Indianapolis, IN, is issuing a voluntary recall of Toxic Waste® Short Circuits™ Bubble Gum, 3.2 oz (90 g) size, Lot #15070SC12 due to elevated levels of lead (0.189 parts per million; the FDA tolerance is 0.1 ppm) that potentially could cause health problems, particularly for infants, small children, and pregnant women. The recalled Short Circuits™ Bubble Gum product was distributed nationwide in retail stores and through mail orders.
http://www.fda.gov/Safety/Recalls/ucm248548.htm
NAC Foods Corporation of Palisades Park, New Jersey is announcing a voluntary recall of the Mi Pepito Arnica Flower and Stem Arnica due to inaccurate usage information on the product label. The current label states ‘Use to enhance the flavor of your favorite dish.’ The label should have stated: ‘Recommended for external use only.’ The product was distributed to retail outlets in Rhode Island, Connecticut, Pennsylvania, New York and New Jersey.
http://www.fda.gov/Safety/Recalls/ucm248703.htm
APP Pharmaceuticals, Inc., (APP) announced today that it has issued a voluntary recall of five lots of Irinotecan Hydrochloride Injection, which is used for recurrent or progressive metastatic colorectal cancer. decided to take this action due to an atypical trend in customer complaints associated with lot 870DE00301.
http://www.fda.gov/Safety/Recalls/ucm248576.htm
USA Far Ocean Group Inc., 1609 W. Valley Blvd., #338, Alhambra, CA 91803, announced today that it is conducting a voluntary nationwide recall of the Company's two supplement products sold under the names X-Hero and Male Enhancer. The Company has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of X-Hero sample found the product contains sulfosildenafil. These two products have been distributed nationwide via retail stores, internet sales and mail order.
http://www.fda.gov/Safety/Recalls/ucm248718.htm
Greenstone LLC announced today that it is voluntarily conducting a recall, to the patient level, of medicines with lot number FI0510058-A on the label. This includes Citalopram 10mg Tablets (100-count bottle) and Finasteride 5mg Tablets (90-count bottle), both distributed in the U.S. market. The recall is due to the possibility that incorrect labels have been placed on the bottles by a third-party manufacturer.
http://www.fda.gov/Safety/Recalls/ucm248552.htm
If you missed last week's recall listing, here is the link to it:
http://www.car-seat.org/showthread.php?t=164785
