at the time everything started to slide downward in 2007, the Canadian company was one of the biggest wet dog and cat food maker in all of North America. Because there are no real reporting systems for animals that get sick or die, it wasn't until vets around the country ...
July 21, 2022 -- Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being...
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. STERILE PRODUCTSNDC ALUMINUM POTASSIUM SULFATE CONCENTRATED (PF) 300 G/300 ML 05446-0637-03 BUFFERED LIDOCAINE HCL (PF) 1% 05446-0850-10 BUFFERED LIDOCAINE HCL / EPINEPHRINE SOLUTION (PF) 1% / 1:100...
The US Food and Drug Administration (FDA) has classified this recall as class I, the most serious type, because of the potential for serious injury or death. "If the device separates during use this may cause serious adverse events such as removal of the separated tip from the carotid arter...
Get free dog food recall alerts sent to you by email. Subscribe to The Dog Food Advisor’s emergency recall notification system. Important Update July 3, 2020 It appears the FDA may have been premature in warning the public about the possible link between DCM and grain-free diet...
The US Food and Drug Administration (FDA) hasissued a Class I labelfor the recall of Medtronic’s MiniMed insulin pumps. Medtronic released asafety noticeback in July implicatingmore than 785,000 pumpsdue to the potential of damaged electrical components, including its battery, after physical imp...
Food and Drug Administration has been working with partners across the U.S. government, academia and industry to expedite the development and availability of critical medical products to treat this novel virus. Today, we are providing an update on one potential treatment called convalescent plasma ...
Food and Drug Administration (FDA) released a joint plan to identify areas of ambiguity, gaps, or uncertainty in their coordinated regulation of biotechnology products. Consistent with a directive issued by President Biden in September 2022, the agencies’ plan identifies specific issues that each ...
This makes the FDA 21 CFR part 11 more relevant than ever – applying to companies under the consumer goods segment, such as drug makers, biotech companies, food manufacturers, cosmetics companies, and other FDA-regulated organizations that have adapted electronic signatures as part of their ...
(e.g., 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, nuts, rawhide chews, or pet treats sold in bulk and fresh fruits and vegetables ...