PET FOOD RECALLED OVER POSSIBLE SALMONELLA, LISTERIA CONTAMINATION 2. Class II recall A product that is classified under a Class II recall could still inflict harm on consumers, but is less serious than a Class I recall. A Class II recall is "a situation in which use of or exposure to a...
Rockville, Md. -- The list of recalled products containing peanut derivatives, compiled by the U.S. Food and Drug Administration, has grown over the last few days, with seven additional pet-food products being added.\ndvm.com staffhttps://www.facebook.com/dvm360...
Beware, pet owners: Some dog food is facing a recall because it may be contaminated with salmonella and listeria, according to a recall notice posted to the Food and Drug Administration’s website this week.
specific retail store name and address) when recalled human or animal food is not easily identified as being the subject of a recall from its retail packaging or lack thereof (e.g., deli cheese,
The FDA announced the Sportmix pet food recall on December 30, after determining certain lots of the dry pet food may contain higher than acceptable levels of aflatoxins, which are poisonous carcinogens and mutagens produced by certain molds. At least 28 dog deaths and eight dog injuries were ...
Food and Drug Administration (FDA) has issued a recall of the Hologic Inc. BioZorb marker due to ... May 22, 2024 News | FDA Indica Labs Receives First FDA Clearance for HALO AP Dx Digital Pathology Platform May 14, 2024 — Indica Labs, the leading provider of digital pathology ...
The U.S. Food and Drug Administration (FDA) has regulatory oversight for substances added to food, including monitoring their safe use.
Many diabetics choose to use an insulin pump to make managing all this easier, but as a recent recall of insulin pump software by the US Food and Drug Administration shows, technology isn’t foolproof. Thankfully, the recall is very narrow in scope. It’s targeted at users of the Tandem...
The recall comes years after surgeons say they first noticed problems with the HeartMate II and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories.
“If consumers have any product with the indicated UPC code and ‘Best if Used By’ dates, they should return it to the place of purchase for a full refund or exchange,” according to Del Monte’s recall notice.(source) If you have more questions, you can contact Del Monte by calling...