Ready-to-eat grilled chicken breast fillets have been recalled in seven states by Suzanna’s Kitchen because of possible contamination with listeria monocytogenes, according to an announcement made by ...
"The court concludes that the Graham complaint does not fall within the 'very limited circumstances' that would establish fraudulent joinder. Philips did not meet its heavy burden to show, as a matter ...
Nearly 40,000 gallons of water sold in six states were recalled after a "floating black foreign substance" was discovered in the product. A recent recall of over 38,000 gallons of Meijer Steam ...
The FDA reclassified the recall as Class I on Jan. 6, nearly two months after first classifying the recall FDA Ambriola Company's recall of select Pecorino Romano cheese products has been reclassified ...
Unsurprisingly, Ford leads the 2025 NHTSA list after recalling over 12 million vehicles, followed by Japanese rival Toyota. Ford recalled the most vehicles in 2025, surpassing 12.9 million units. High ...
In a year that will go down as one of the most active ever for auto safety actions, 2025 produced an extraordinary number of vehicle recall campaigns across the U.S. automotive industry. According to ...
Ford Motor Company logged far more recalls in 2025 than any other automaker, according to federal safety data, eclipsing a decade-old industry record and underscoring ongoing quality issues affecting ...
Over 83,000 bags of raw shrimp from Indonesia are being recalled, the FDA said. The FDA has announced a recall of frozen raw shrimp due to potential exposure to the radioactive isotope cesium-137. The ...
PITTSBURGH — A Pennsylvania federal court remanded a California woman’s negligence complaint over injuries allegedly caused by a recalled Philips CPAP device back to Los Angeles County Superior Court.
A voluntary recall has been issued for pints of a non-dairy frozen dessert over the potential presence of small stones and other hard objects, according to the Food and Drug Administration. Danone U.S ...
Add Yahoo as a preferred source to see more of our stories on Google. Several batches of the drug did not dissolve properly, which means the person taking them would receive a lower dose.
The FDA’s oversight of medical device recalls continues to be plagued by staffing challenges—forcing some activities to be placed on the “back burner” and resulting in lengthy response times, ...