MomToEliEm
Moderator
Here is a list of new product recalls issued this week: 10/05/13-10/21/13
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 allergens. To view all the recalls including those allergen related recalls, you can go to: http://www.recalls.gov/recent.html to see a full listing from each agency.
Costco’s El Camino Real store in South San Francisco, Calif., is recalling 23,138 units (approximately 39,755 lbs.) of rotisserie chicken products (“Kirkland Signature Foster Farms”, “Kirkland Farm”) that may be contaminated with a strain of Salmonella Heidelberg
http://www.fsis.usda.gov/wps/wcm/co...archive/archive/2013/recall-058-2013-expanded
Garden Fresh Foods, a Milwaukee, WI. establishment, is recalling approximately 6,694 additional pounds of ready-to-eat chicken and ham products due to possible contamination with Listeria monocytogenes. The company is recalling these products in addition to the 19,054 pounds of similar products that were recalled on Sept. 25, 2013. The products being recalled bear the establishment number “EST. 17256” or “Est. P-17256” inside the USDA mark of inspection, and were distributed to retail and food service establishments nationwide.
http://www.fsis.usda.gov/wps/wcm/co...archive/archive/2013/recall-055-2013-expanded
Orange County Produce, LLC ("OC Produce") is voluntarily working with the Food and Drug Administration ("FDA") and California Department of Public Health ("CDPH") to coordinate a recall of fresh red and green Bell Peppers for potential contamination with Salmonella. The lots were distributed to farmer's markets and wholesale food service within Southern California between September 21 and September 24, 2013.
http://www.fda.gov/Safety/Recalls/ucm370801.htm
Turkey Hill Dairy of Conestoga, Pa., is recalling specific packages of 1.5 qt. (48 oz./1.42L) of Fudge Ripple Premium Ice Cream and 1 Pint (16 oz./473 ml) packages of Chocolate Peanut Butter Cup Premium Ice Cream, and Moose Tracks® Stuff’d Frozen Dairy Dessert due to the possibility that some packages may contain metal shavings. The recalled items are limited to packages sold at select Turkey Hill Minit Markets in Pennsylvania, select Wal-Marts in Pennsylvania and West Virginia, and other small grocers and convenience stores in Maryland and Pennsylvania.
http://www.fda.gov/Safety/Recalls/ucm370820.htm
Asia Cash & Carry Inc. of Maspeth, New York is voluntarily recalling PRAN brand Spice Powder TURMERIC, Net Wt. 8.82 oz. (250 gm) jars, because it was found to contain high levels of lead. PRAN brand Spice Powder TURMERIC was distributed in New York, Pennsylvania, Massachusetts, Virginia, and Illinois through retail stores.
http://www.fda.gov/Safety/Recalls/ucm370854.htm
BEST VALUE, INC. of Detroit, MI is voluntarily recalling PRAN TURMERIC POWDER because it was found to contain high levels of lead. It was distributed in and around Hamtramck, Michigan through retail stores.
http://www.fda.gov/Safety/Recalls/ucm371042.htm
FAHMAN ENTERPRISES INC. of Dallas, TX is voluntarily recalling PRAN TURMERIC POWDER because it was found to contain high levels of lead . The recalled product was distributed in the city of Dallas, TX to retail stores between the dates of July 2013 to September 2013.
http://www.fda.gov/Safety/Recalls/ucm371206.htm
Hospira, Inc. (NYSE: HSP), announced today it will initiate a voluntary nationwide recall to the user level for one lot of 0.25% Marcaine™ (Bupivacaine HCl Injection, USP), 75 mg/30 mL, Single-dose Vial – Preservative Free (NDC 0409-1559-30), Lot 25-220-DD. The recall is due to a confirmed customer report of discolored solution with visible particles inside the glass vial as well as embedded in the glass.
http://www.fda.gov/Safety/Recalls/ucm371412.htm
Specialty Medicine Compounding Pharmacy is voluntarily recalling all lots of certain unexpired human and veterinary sterile products to the consumer level due to particulate matter found in vials of a compounded dextrose injection product dispensed to a local hospital. The recalled products were distributed to hospitals and consumers located only within Michigan from July 1, 2013, through October 19, 2013.
http://www.fda.gov/Safety/Recalls/ucm371436.htm
Nephron Pharmaceuticals Corporation Announces Voluntary Recall of Albuterol Sulfate Inhalation Solution, 0.083%.
http://www.fda.gov/Safety/Recalls/ucm371151.htm
B@B Trade, Inc., Florida is voluntarily recalling all lots of Slim Fortune, Lidiy, and Slim Expert to the consumer level. The FDA laboratory analysis of these dietary supplements found to contain undeclared Sibutramine. The products were sold directly to individual customers in our Florida, sales office and online at www.lidiy.com, www.slimfortune.com, or www.slimexpert.com.
http://www.fda.gov/Safety/Recalls/ucm370884.htm
B. Braun Medical Inc. (B.Braun) is voluntarily recalling one lot of 1g Cefepime for Injection USP and Dextrose Injection USP (Lot H3A744, catalog 3193-11) to the consumer level. The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample unit.
http://www.fda.gov/Safety/Recalls/ucm371030.htm
GE Healthcare has initiated a voluntary field corrective action for the Avance, Aisys and Avance CS2 anesthesia delivery systems with 8.00 (Avance and Aisys) or 10.00 (Avance CS2) software due to a potential safety issue. The affected units were manufactured from February 2011 through July 2013.
http://www.fda.gov/Safety/Recalls/ucm371037.htm
If you missed last week's recall listing, here is the link to it:
http://www.car-seat.org/showthread.php?t=256617
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 allergens. To view all the recalls including those allergen related recalls, you can go to: http://www.recalls.gov/recent.html to see a full listing from each agency.
Costco’s El Camino Real store in South San Francisco, Calif., is recalling 23,138 units (approximately 39,755 lbs.) of rotisserie chicken products (“Kirkland Signature Foster Farms”, “Kirkland Farm”) that may be contaminated with a strain of Salmonella Heidelberg
http://www.fsis.usda.gov/wps/wcm/co...archive/archive/2013/recall-058-2013-expanded
Garden Fresh Foods, a Milwaukee, WI. establishment, is recalling approximately 6,694 additional pounds of ready-to-eat chicken and ham products due to possible contamination with Listeria monocytogenes. The company is recalling these products in addition to the 19,054 pounds of similar products that were recalled on Sept. 25, 2013. The products being recalled bear the establishment number “EST. 17256” or “Est. P-17256” inside the USDA mark of inspection, and were distributed to retail and food service establishments nationwide.
http://www.fsis.usda.gov/wps/wcm/co...archive/archive/2013/recall-055-2013-expanded
Orange County Produce, LLC ("OC Produce") is voluntarily working with the Food and Drug Administration ("FDA") and California Department of Public Health ("CDPH") to coordinate a recall of fresh red and green Bell Peppers for potential contamination with Salmonella. The lots were distributed to farmer's markets and wholesale food service within Southern California between September 21 and September 24, 2013.
http://www.fda.gov/Safety/Recalls/ucm370801.htm
Turkey Hill Dairy of Conestoga, Pa., is recalling specific packages of 1.5 qt. (48 oz./1.42L) of Fudge Ripple Premium Ice Cream and 1 Pint (16 oz./473 ml) packages of Chocolate Peanut Butter Cup Premium Ice Cream, and Moose Tracks® Stuff’d Frozen Dairy Dessert due to the possibility that some packages may contain metal shavings. The recalled items are limited to packages sold at select Turkey Hill Minit Markets in Pennsylvania, select Wal-Marts in Pennsylvania and West Virginia, and other small grocers and convenience stores in Maryland and Pennsylvania.
http://www.fda.gov/Safety/Recalls/ucm370820.htm
Asia Cash & Carry Inc. of Maspeth, New York is voluntarily recalling PRAN brand Spice Powder TURMERIC, Net Wt. 8.82 oz. (250 gm) jars, because it was found to contain high levels of lead. PRAN brand Spice Powder TURMERIC was distributed in New York, Pennsylvania, Massachusetts, Virginia, and Illinois through retail stores.
http://www.fda.gov/Safety/Recalls/ucm370854.htm
BEST VALUE, INC. of Detroit, MI is voluntarily recalling PRAN TURMERIC POWDER because it was found to contain high levels of lead. It was distributed in and around Hamtramck, Michigan through retail stores.
http://www.fda.gov/Safety/Recalls/ucm371042.htm
FAHMAN ENTERPRISES INC. of Dallas, TX is voluntarily recalling PRAN TURMERIC POWDER because it was found to contain high levels of lead . The recalled product was distributed in the city of Dallas, TX to retail stores between the dates of July 2013 to September 2013.
http://www.fda.gov/Safety/Recalls/ucm371206.htm
Hospira, Inc. (NYSE: HSP), announced today it will initiate a voluntary nationwide recall to the user level for one lot of 0.25% Marcaine™ (Bupivacaine HCl Injection, USP), 75 mg/30 mL, Single-dose Vial – Preservative Free (NDC 0409-1559-30), Lot 25-220-DD. The recall is due to a confirmed customer report of discolored solution with visible particles inside the glass vial as well as embedded in the glass.
http://www.fda.gov/Safety/Recalls/ucm371412.htm
Specialty Medicine Compounding Pharmacy is voluntarily recalling all lots of certain unexpired human and veterinary sterile products to the consumer level due to particulate matter found in vials of a compounded dextrose injection product dispensed to a local hospital. The recalled products were distributed to hospitals and consumers located only within Michigan from July 1, 2013, through October 19, 2013.
http://www.fda.gov/Safety/Recalls/ucm371436.htm
Nephron Pharmaceuticals Corporation Announces Voluntary Recall of Albuterol Sulfate Inhalation Solution, 0.083%.
http://www.fda.gov/Safety/Recalls/ucm371151.htm
B@B Trade, Inc., Florida is voluntarily recalling all lots of Slim Fortune, Lidiy, and Slim Expert to the consumer level. The FDA laboratory analysis of these dietary supplements found to contain undeclared Sibutramine. The products were sold directly to individual customers in our Florida, sales office and online at www.lidiy.com, www.slimfortune.com, or www.slimexpert.com.
http://www.fda.gov/Safety/Recalls/ucm370884.htm
B. Braun Medical Inc. (B.Braun) is voluntarily recalling one lot of 1g Cefepime for Injection USP and Dextrose Injection USP (Lot H3A744, catalog 3193-11) to the consumer level. The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample unit.
http://www.fda.gov/Safety/Recalls/ucm371030.htm
GE Healthcare has initiated a voluntary field corrective action for the Avance, Aisys and Avance CS2 anesthesia delivery systems with 8.00 (Avance and Aisys) or 10.00 (Avance CS2) software due to a potential safety issue. The affected units were manufactured from February 2011 through July 2013.
http://www.fda.gov/Safety/Recalls/ucm371037.htm
If you missed last week's recall listing, here is the link to it:
http://www.car-seat.org/showthread.php?t=256617
