Feed Solutions has initiated a voluntary recall of certain varieties of the feed products with specific lot codes listed below, due to the potential for elevated vitamin D levels. Elevated vitamin D levels may cause death or otherwise be harmful to animals and fish if fed for extended periods, potentially resulting in lack of interest in eating, … [Read more...]
PMI Nutrition International Initiates Voluntary Recall of AquaMax™ Products; Expands Voluntary Recall of Mazuri® and LabDiet®Feed Products Due to Potential Elevated Vitamin D Level
PMI Nutrition International is initiating a voluntary recall of certain varieties of the AquaMax™ feed products with specific lot codes listed below, due to the potential for elevated vitamin D levels. Although no customer complaints have been received to date, the products are being recalled due to analytical test results that indicate a potential … [Read more...]
Hospira Announces A Nationwide Recall of Certain Lots of Injectable Carboplatin, Cytarabine, Paclitaxel and Methotrexate Due to Glass Vial Defect
Hospira, Inc. (NYSE: HSP), the world's leading provider of injectable drugs and infusion technologies, issued this press release today to further inform the general public about a previously communicated user level recall of a total of 19 lots of carboplatin, cytarabine, paclitaxel, and methotrexate (see table below) in the United States due to … [Read more...]
Chicco Polly High Chairs Recalled Due to Laceration Hazard
p>WASHINGTON, D.C. - 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 … [Read more...]
Family Dollar Stores Recalls Decorative Light Sets Due To Fire and Electrical Shock Hazard
WASHINGTON, D.C. - 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 … [Read more...]
Old Navy Recalls Toddler Girl Aqua Socks Due to Slip and Fall Hazard
p>WASHINGTON, D.C. - 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 … [Read more...]
Molenaar Recalls Folding Step Stools Due to Fall Hazard
WASHINGTON, D.C. - 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 … [Read more...]
ZERO ( 12V310000 )
Vehicle Make / Model: Model Year(s): ZERO / ZERO DS 2012 ZERO / ZERO S 2012 ZERO / ZERO X 2012 ZERO / ZERO XU 2012 ZERO … [Read more...]
CAMPAGNA ( 12V322000 )
Vehicle Make / Model: Model Year(s): CAMPAGNA / V13R 2011-2012 Manufacturer: CAMPAGNA MOTORS Mfr's Report Date: JUN 14, 2012 NHTSA CAMPAIGN ID Number: 12V322000 N/A NHTSA Action Number: N/A Component: SEAT BELTS:FRONT:ANCHORAGE Potential Number of Units Affected: 67 Summary: … [Read more...]
ENTEGRA ( 12V312000 )
Vehicle Make / Model: Model Year(s): ENTEGRA / ANTHEM 2011-2013 ENTEGRA / ASPIRE 2011-2013 ENTEGRA / CORNERSTONE 2012-2013 Manufacturer: ENTEGRA COACH Mfr's Report Date: JUL 03, 2012 NHTSA … [Read more...]
Stryker Recalls ABG II and Rejuvenate Modular-Neck Stems for Risks Posed by Corrosion and Wear
Stryker Orthopaedics has recalled two modular neck stem models for hip implants because of the risk of corrosion and wear, which can cause tissue damage. The devices are the modular-neck hip stems ABG II and Rejuvenate. The risks posed by corrosion can lead to hip implant failure. Pain and swelling at the implant site may indicate adverse tissue … [Read more...]
Troxel Recalls Flexible Flyer Swing Sets Due to Fall Hazard
Troxel has recalled about 100,500 Flexible Flyer Swing Sets in the United States, and 4,900 in Canada because the see saw seat bolt fasteners can break during use. Manufacturer: The Troxel Company, of Moscow, Tenn. Hazard: The see saw seats can break away from the bolt fasteners during use, posing a fall hazard. Incidents/Injuries: The firm … [Read more...]
Nikon Recalls Rechargeable Battery Packs Sold with Digital SLR Cameras Due to Burn Hazard
About 5,100 Nikon digital SLR camera rechargeable battery packs have been recalled in the United States because they can short circuit, causing the batteries to overheat and melt. Incidents/Injuries: Nikon has received seven reports of incidents outside of the U.S. and Canada of the recalled battery packs overheating. No incidents have been … [Read more...]
Mack Truck, 2012 CHU, CXU, and GU Vehicles Recalled
Manufacturer: MACK TRUCKS, INC Mfr's Report Date: JUN 29, 2012 NHTSA CAMPAIGN ID Number: 12V308000 Component: VISIBILITY:WINDSHIELD WIPER/WASHER:LINKAGES Potential Number of Units Affected: 1,174 Summary: MACK IS RECALLING CERTAIN MODEL YEAR 2012 CHU, CXU, AND GU VEHICLES, MANUFACTURED FROM OCTOBER 10, 2011, THROUGH NOVEMBER 17, 2011. … [Read more...]
Updated Sedona Labs Issues A Voluntary Recall For iFlora Kids Multi-Probiotic Dietary Supplement Due to Possible Health Risk
Contact:Consumer:1-888-816-8804Media:Amélie GermainDirector of CommunicationsT : 418 652-1173 x330 ag@atrium-innovations.com FOR IMMEDIATE RELEASE - July 10, 2012 - Sedona Labs today announced that its supplier of Galactooligosaccharide (GOS) has recalled this ingredient due to a possible Salmonella contamination. As a result, we … [Read more...]
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