Belfonte Ice Cream and Dairy Foods Company, due to Sunland, Inc's expanded voluntary recall of Almond Butter, Peanut Butter, Cashew Butter, Tahini and Roasted Blanched Peanut Products, has initiated a recall of a peanut butter containing ice cream produced at our Kansas City, MO plant because it has the potential to be contaminated with Salmonella, … [Read more...]
Clemmy’s is Voluntarily Recalling Peanut Butter Chocolate Chip Ice Cream Due to Possible Health Risks
Clemmy's Ice Cream of Rancho Mirage, CA is initiating a voluntary recall of Peanut Butter Chocolate Chip 16 ounce containers of ice cream that contains peanut butter associated with the Sunland, Inc., recall. The peanut butter used in this product has the potential to be contaminated with Salmonella. Salmonella is an organism which can cause … [Read more...]
Graco Recalls Classic Wood Highchairs Due to Fall Hazard
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...]
Kitchen Fires #1 in New Report; Smoke Alarms and Escape Plans Key to Surviving Fires in the Home
WASHINGTON, D.C. - In recognition of Fire Prevention Week, the U.S. Consumer Product Safety Commission (CPSC) and the U.S. Fire Administration (USFA) are providing new statistics on fires in American homes and urging consumers to install smoke alarms in their homes and check to make sure all smoke alarms are working properly. It is also vitally … [Read more...]
Bliss Unlimited, LLC, Voluntarily Recalls Luna & Larry’s Coconut Bliss Chocolate Peanut Butter Non-Dairy Frozen Dessert, Code Dates Nov 11 2012 – Oct 24 2013, Due To Possible Health Risk
Bliss Unlimited, LLC, Eugene, Oregon is recalling Luna & Larry's Coconut Bliss Chocolate Peanut Butter Non-Dairy Frozen Dessert with codes dates Nov 11 2012 through Oct 24 2013 only. This recall is being initiated because the peanut butter used in the product for these specific code dates is supplied by Sunland, Inc., which has issued a … [Read more...]
Evenflo Company, Inc. Equipment:other:labels Recall
Child Restraint Brand Name / Model or Model No.:EVENFLO / BIG KID Production Dates:Information not Available Manufacturer: EVENFLO COMPANY, INC.Report Receipt Date: SEP 27, 2012NHTSA CAMPAIGN ID Number: 12C003000NHTSA Action Number: N/AComponent: EQUIPMENT:OTHER:LABELSPotential Number of Units Affected: 151Summary:Certain Evenflo Big Kid … [Read more...]
Morgan Olson Corporation Visibility:defroster/defogger System Recall
Vehicle Make / Model:MORGAN OLSON / WALK IN VAN Model Year(s):2009-2012 Manufacturer: Morgan Olson CorporationReport Receipt Date: SEP 03, 2012NHTSA CAMPAIGN ID Number: 12V482000NHTSA Action Number: N/AComponent: VISIBILITY:DEFROSTER/DEFOGGER SYSTEMPotential Number of Units Affected: 24Summary:Morgan Olson is recalling certain model year … [Read more...]
Morgan Olson Corporation Latches/locks/linkages:doors:latch Recall
Vehicle Make / Model:MORGAN OLSON / WALK IN VAN Model Year(s):2009-2011 Manufacturer: MORGAN OLSON CORPORATIONReport Receipt Date: JAN 19, 2012NHTSA CAMPAIGN ID Number: 12V021000NHTSA Action Number: N/AComponent: LATCHES/LOCKS/LINKAGES:DOORS:LATCHPotential Number of Units Affected: 7,853Summary:Morgan Olson is recalling certain model … [Read more...]
Nina International Recalls Ground Hot Pepper Because Of Possible Health Risk
Out of the utmost caution and care for our customers, Nina International of Hyattsville, MD is initiating a voluntary recall of its brand of Ground Hot Pepper, 5oz, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and … [Read more...]
Yokohama Tire Corporation Tires:sidewall Recall
Tire Brand Name / Tire Line / Tire Size:YOKOHAMA / AVID TOURING S / 215/65R16 Production Dates:FEB 15, 2009 - APR 18, 2009 Manufacturer: YOKOHAMA TIRE CORPORATIONReport Receipt Date: OCT 02, 2012NHTSA CAMPAIGN ID Number: 12T025000NHTSA Action Number: N/AComponent: TIRES:SIDEWALLPotential Number of Units Affected: 10,669Summary:Yokohama … [Read more...]
Sharper Image USB Wall Chargers Recalled by Atomi Due to Fire and Burn Hazards
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...]
Voluntary Recall of Select Packages of Frosted Mini-Wheats Bite Size Original and Mini-Wheats Unfrosted Bite Size
We have initiated a voluntary recall due to the possible presence of fragments of flexible metal mesh from a faulty manufacturing part. Recalled products include only Frosted Mini-Wheats Bite Size Original and Mini-Wheats Unfrosted Bite Size with the letters KB, AP or FK before or after the Best If Used Before date. Products impacted are: Kellogg's … [Read more...]
DePuy Hip Recall Litigation Update
The U.S. Judicial Panel on Multidistrict Litigation established a DePuy Orthopaedics ASRMultidistrict Litigation (MDL) number 2197 in U.S District Court, Northern District of Ohio on December 7, 2010. The Northern District of Ohio is a federal court, and the MDL centralizes all the DePuy hip recall cases in federal court. At the time of the … [Read more...]
DePuy Hip System Recall Information
In August 2010, DePuy Orthopaedics issued a voluntary recall of its ASR Hip System, a metal-on-metal hip implant system, because a higher number of patients than previously reportedsuffered from pain, swelling, and difficulties walking. This system was first available in July 2003and was marketed in the United States starting in 2005. The ASR Hip … [Read more...]
Body Basics Inc. Recalls ACTRA-Sx 500 Capsules, Lot 008-A
Body Basics Inc. has recalled ACTRA-Sx 500 Dietary Supplement Capsules, Lot 008-A, Expiration December 2013. The Company, through independent lab analysis has confirmed the presence of Sildenafil Citrate making this product unapproved new drugs. Sildenafil is the active ingredient used in an FDA approved drug to treat Erectile Dysfunction (ED). The … [Read more...]
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