Product Recall Updated: August 29, 2024 Share: When a product has widespread incidents or has been improperly labeled, then it may be necessary to undergo a product recall. But what exactly is a product recall? Read on as we take a closer look. ...
This recall is a result of sampling by the State of Maryland that found samples from one production lot of Martinelli’s apple juice, sold in one-liter glass bottles, tested above the guidance action level for inorganic arsenic in apple juice set by the FDA in June 2023. FDA has stated ...
According to FDA guidance, when the product has already been distributed to the consumer level and there is a potential for a significant health hazard, a press release is considered appropriate. The FDA publishes these press releases on their website and has archived press releases for recall ...
Fungal contamination of an eye product is known to potentially cause eye infections, which may be vision- or life-threatening, according to the FDA. Dec 27, 2024 Pet food brand issues recall over bird flu contamination A voluntary recall was issued for a line of raw and frozen pet ...
RECALL: FCA Updates Action For OVER 700k Minivans — New Guidance Issued3/10/15"If the ignition key inadvertently moves into the OFF or ACCESSORY position, the engine will turn off, which will then depower various key safety systems including but not limited to air bags, power steering, and...
Tandem updates recall of mobile app causing rapid battery depletion of insulin pumps Tandem Diabetes Care emailed notices to users of version 2.7.1 of the Apple iOS t:connect mobile app warning of possible rapid battery depletion of their insulin pump, according to an FDA press release. ...
FDA testing found "extremely high levels of lead contamination" in the cinnamon applesauce pouches, which have been recalled. Jan 24, 2024 Ford recalls nearly 1.9 million Explorer SUVs over loose trim pieces The recall comes a year after U.S. safety regulators determined the problem to be a ...
FDA's device center has significantly sped up the process for terminating class I product recalls at a time when the number of those high-risk corrections and removals continues to grow. CDRH terminates a class I recall after it determin... SM Schmitt - 《Silver Sheet Medical Devices Design ...
can initiate a voluntary recall themselves.) The FDA provides aproduct recall guidance documenton what to do if faced with a product removal from the market. The guidance includes a checklist of documentation and information that the FDA uses to evaluate, classify, monitor and audit product ...
This recall is a result of sampling by the State of Maryland that found samples from one production lot of Martinelli’s apple juice, sold in one-liter glass bottles, tested above the guidance action level for inorganic arsenic in apple juice set by the FDA in June 2023. FDA has stated ...