Comeaux's Inc., a Breaux Bridge, La. establishment, is recalling approximately 14 pounds of pork products that may be adulterated with Listeria monocytogenes. … [Read more...]
KTM North America Recalls Competition/Closed Course Off-Road Motorcycles Due to Fire Hazard (Recall Alert)
The molded fuel hoses could leak fuel at the radius or the ends of the hose, posing a fire hazard. … [Read more...]
Huisken Meat Company Recalls Beef Products Due To Possible Foreign Matter Contamination
Huisken Meat Company, a Sauk Rapids, Minn. establishment, is recalling approximately 89,568 pounds of beef products that may be contaminated with extraneous wood materials. … [Read more...]
Baxter Initiates Voluntary Recall of Two Lots of IV Solutions due to Potential Presence of Particulate Matter
Baxter International Inc. announced today it is voluntarily recalling two lots of intravenous (IV) solutions to the hospital/end user level due to the potential presence of particulate matter. The particulate matter in each case was determined to be an insect and was identified as a result of a customer complaint. … [Read more...]
Big Dog Natural Recalls Chicken and Fish Supreme Dog Food Due to Possible Salmonella and Listeria monocytogenes Health Risk
Big Dog Natural of Brick, NJ is voluntary recalling a select production lot of Big Dog Natural raw dehydrated dog food Chicken Supreme potentially contaminated with Salmonella and Fish Supreme potentially contaminated with Listeria monocytogenes that was shipped in the week of 10/31/2015 to 11/13/2015 to online customers. Salmonella and Listeria … [Read more...]
Du Monde Gourmet Recalls Jafflz Sandwich Products Due To Possible Cooling/Process Deviation
WASHINGTON, Dec. 31, 2015 – Du Monde Gourmet, a Park City, UT establishment, is recalling approximately 235 pounds of ready-to-eat pocket sandwich products, which may have experienced temperature deviation and may contain Clostridium perfringens, Bacillus cereus, and/or Clostridium botulinum. … [Read more...]
Pharmedium Issues Voluntary Nationwide Recall of 4mg Norepinephrine Bitartrate (16mcg/mL) Added to 0.9% Sodium Chloride in 250mL Viaflex Bag and 8mg Norepinephrine Bitartrate (32mcg/mL) Added to 0.9% Sodium Chloride in 250mL Viaflex Bag for Discoloration.
Lake Forest, IL PharMEDium Services, LLC is voluntarily recalling 29 lots of 4mg Norepinephrine Bitartrate (16mcg/mL) added to 0.9% Sodium Chloride in 250mL Viaflex Bag and 3 lots of 8mg Norepinephrine Bitartrate (32mcg/mL) added to 0.9% Sodium Chloride in 250mL Viaflex Bag distributed to hospital customers. We have received complaints from … [Read more...]
Thomas Produce Recalls Cucumbers because of Possible Health Risk
Thomas Produce Company of Boca Raton, FL is recalling 174 bulk-packed containers of Cucumbers. This product 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 others with weakened immune systems. … [Read more...]
KTM North America Recalls Competition Off-Road Motorcycles Due to Fire Hazard (Recall Alert)
Under extreme riding conditions, fuel can escape from the tank breather assembly. This poses a risk of fire and injury to the rider. … [Read more...]
Origin8 Recalls Folding Bicycles Due to Fall Hazard
The frame on the folding bicycles can break, posing a fall hazard. … [Read more...]
Macy’s Recalls Martha Stewart Stainless Steel Cookware; Injury Hazard with Frying Pans
The metal discs that cover the frying pan’s rivets can pop off and hit consumers, posing an injury hazard. … [Read more...]
Uoriki Fresh, Inc. Recalls "Octopus Salad" Because of Possible Health Risk
Uoriki Fresh, Inc. (UF) of Secaucus, NJ is recalling its "Octopus Salad", because it has the potential to be contaminated with Listeria monocytogenes (LA1) , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer … [Read more...]
Medical Device Makers Fail to Complete Post-Approval Studies
The U.S. Food and Drug Administration (FDA) approval process can be so slow that people die waiting for potentially life-saving drugs and medical devices that are fully developed, but not yet available. One way to get devices to people sooner is the FDA’s post-approval studies program (PAS). It requires far less from device makers before approval, … [Read more...]
Taylor Farms Pacific, Inc. Recalls Signature Cafe Traditional Stuffing Due to Potential Undeclared Allergens
Taylor Farms Pacific, Inc. of Tracy, California is voluntarily recalling 190 cases of Signature Cafe Traditional Stuffing because the product label did not identify certain ingredients including soy, milk and wheat. The recalled product was sold in a limited number of Safeway and Pak 'N Save stores in Northern California and Nevada and Vons stores … [Read more...]
Nuway Distributors llc Issues Voluntary [Worldwide/Nationwide] Recall of APEXXX Due to Presence of Undeclared Slidenafil
Nuway Distributors llc is voluntarily recalling all lots of APEXXX tablets to the consumer level. FDA analysis found APEXXX to contain amounts of the PDE-5 Inhibitor, sildenafil, which is the active ingredient in an FDA-approved drug for erectile dysfunction (ED) making this tainted dietary supplement and unapproved drug. … [Read more...]
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