MomToEliEm
Moderator
Here is a list of new product recalls issued this week: 08/06/10-08/13/10
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.
P. Graham Dunn Recalls Wooden Toy Rattles Due to Choking Hazard. Sold by: Gift stores and book retailers nationwide from June 2010 through July 2010 for about $6.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10317.html
Circus World Recalls Levana Wireless Video Baby Monitors Due to Overheating Hazard. Sold at: BB Buggy and Health and Safety stores nationwide and on the Internet between February 2010 and May 2010 for about $200.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10318.html
Asurion Recalls Counterfeit BlackBerry®-branded cell phone batteries in refurbished devices Due to Burn and Fire Hazards. Distributed through: Asurion as part of their handset protection claim program nationwide from March 2004 through October 2009.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10752.html
LG Electronics Reissues Recall on Goldstar and Comfort-Aire Portable Dehumidifier Due to Additional Reports of Fires and Low Consumer Response Rate. Sold at: The Home Depot, Walmart and Heat Controller Inc. nationwide from January 2007 through June 2008 for between $140 and $150.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10316.html
Bosch Thermotechnology Recalls Boiler Survey Kits For Gas-Fired Boiler Due to Fire Hazard. Distributed to: Plumbing and heating contractors and equipment distributors nationwide from February 2010 through May 2010 for free.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10751.html
Fresh Express is voluntarily recalling 2,825 cases of Veggie Lovers Salad with a Product Code of I208 and Use-by Date of August 10, 2010 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. Product was distributed to the following states: MO, MI, OH, IL, WI, IN, MD, MA, NY, KS, KY, PA, NJ. There is a possibility of redistribution to the following states: AR, TN, WV, IA, MN, DC, VA, VT, NH, NE, RI, PA, CT, MS
http://www.fda.gov/Safety/Recalls/ucm221943.htm
Goya Foods, Inc. of Secaucus, NJ, is recalling its 14 ounce packages of Frozen Mamey Pulp, due to a potential health risk from Salmonella. The recalled Goya brand Mamey Pulp was distributed in the states of AK, AZ, CA, CO, HI, NM, NV, OR, TX, UT, and WA through retail stores.
http://www.fda.gov/Safety/Recalls/ucm222223.htm
EZVille, Ltd. of Ronkonkoma, NY, has been informed by the US Food and Drug Administration (FDA) that FDA lab analysis of Revivexxx® Extra Strength distributed by the company was found to contain undeclared tadalafil. Tadalafil is an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making Revivexxx® Extra Strength an unapproved drug. The product was sold to distributors and retail stores nationwide and via internet sales.
http://www.fda.gov/Safety/Recalls/ucm221663.htm
EZVille, Ltd. of Ronkonkoma, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Solo Slim® distributed by the company was found to contain an undeclared drug ingredient. Solo Slim® was found to contain Didesmethyl Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The products were sold to distributors and retail stores nationwide and via internet sales.
http://www.fda.gov/Safety/Recalls/ucm221660.htm
Prolatis’ is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found Prolatis’ to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED), making Prolatis’ an unapproved drug.
http://www.fda.gov/Safety/Recalls/ucm222315.htm
Novacare LLC announced today that it is conducting a voluntary nationwide recall of products sold under the following names: Stiff Nights, Aziffa, Size Matters, Erex, Mojo, Hard Drive, Eyeful, Red Magic, Straight Up, Zotrex, Monster Excyte, WOW, Xaitrex, Verect, Prolatis, Xytamax, Maxyte, Libidinal, OMG, OMG45, and Zilex (with Golden Spear). Novacare LLC has been informed by representatives of the Food & Drug Administration (FDA) that the products appear to contain sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction.
http://www.fda.gov/Safety/Recalls/ucm221958.htm
Ikaria, Inc. announced today that its INOMAX® DS drug-delivery systems in the United States are being voluntarily recalled due to the potential failure of a pressure switch which may have an impact on the administration of INOMAX® (nitric oxide) for inhalation to patients.
http://www.fda.gov/Safety/Recalls/ucm221940.htm
If you missed last week's recall listing, here is the link to it:
http://www.car-seat.org/showthread.php?t=136460
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.
P. Graham Dunn Recalls Wooden Toy Rattles Due to Choking Hazard. Sold by: Gift stores and book retailers nationwide from June 2010 through July 2010 for about $6.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10317.html
Circus World Recalls Levana Wireless Video Baby Monitors Due to Overheating Hazard. Sold at: BB Buggy and Health and Safety stores nationwide and on the Internet between February 2010 and May 2010 for about $200.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10318.html
Asurion Recalls Counterfeit BlackBerry®-branded cell phone batteries in refurbished devices Due to Burn and Fire Hazards. Distributed through: Asurion as part of their handset protection claim program nationwide from March 2004 through October 2009.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10752.html
LG Electronics Reissues Recall on Goldstar and Comfort-Aire Portable Dehumidifier Due to Additional Reports of Fires and Low Consumer Response Rate. Sold at: The Home Depot, Walmart and Heat Controller Inc. nationwide from January 2007 through June 2008 for between $140 and $150.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10316.html
Bosch Thermotechnology Recalls Boiler Survey Kits For Gas-Fired Boiler Due to Fire Hazard. Distributed to: Plumbing and heating contractors and equipment distributors nationwide from February 2010 through May 2010 for free.
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10751.html
Fresh Express is voluntarily recalling 2,825 cases of Veggie Lovers Salad with a Product Code of I208 and Use-by Date of August 10, 2010 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. Product was distributed to the following states: MO, MI, OH, IL, WI, IN, MD, MA, NY, KS, KY, PA, NJ. There is a possibility of redistribution to the following states: AR, TN, WV, IA, MN, DC, VA, VT, NH, NE, RI, PA, CT, MS
http://www.fda.gov/Safety/Recalls/ucm221943.htm
Goya Foods, Inc. of Secaucus, NJ, is recalling its 14 ounce packages of Frozen Mamey Pulp, due to a potential health risk from Salmonella. The recalled Goya brand Mamey Pulp was distributed in the states of AK, AZ, CA, CO, HI, NM, NV, OR, TX, UT, and WA through retail stores.
http://www.fda.gov/Safety/Recalls/ucm222223.htm
EZVille, Ltd. of Ronkonkoma, NY, has been informed by the US Food and Drug Administration (FDA) that FDA lab analysis of Revivexxx® Extra Strength distributed by the company was found to contain undeclared tadalafil. Tadalafil is an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making Revivexxx® Extra Strength an unapproved drug. The product was sold to distributors and retail stores nationwide and via internet sales.
http://www.fda.gov/Safety/Recalls/ucm221663.htm
EZVille, Ltd. of Ronkonkoma, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Solo Slim® distributed by the company was found to contain an undeclared drug ingredient. Solo Slim® was found to contain Didesmethyl Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The products were sold to distributors and retail stores nationwide and via internet sales.
http://www.fda.gov/Safety/Recalls/ucm221660.htm
Prolatis’ is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found Prolatis’ to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED), making Prolatis’ an unapproved drug.
http://www.fda.gov/Safety/Recalls/ucm222315.htm
Novacare LLC announced today that it is conducting a voluntary nationwide recall of products sold under the following names: Stiff Nights, Aziffa, Size Matters, Erex, Mojo, Hard Drive, Eyeful, Red Magic, Straight Up, Zotrex, Monster Excyte, WOW, Xaitrex, Verect, Prolatis, Xytamax, Maxyte, Libidinal, OMG, OMG45, and Zilex (with Golden Spear). Novacare LLC has been informed by representatives of the Food & Drug Administration (FDA) that the products appear to contain sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction.
http://www.fda.gov/Safety/Recalls/ucm221958.htm
Ikaria, Inc. announced today that its INOMAX® DS drug-delivery systems in the United States are being voluntarily recalled due to the potential failure of a pressure switch which may have an impact on the administration of INOMAX® (nitric oxide) for inhalation to patients.
http://www.fda.gov/Safety/Recalls/ucm221940.htm
If you missed last week's recall listing, here is the link to it:
http://www.car-seat.org/showthread.php?t=136460
