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2 min read. Aug. 26, 2024 – The FDA announced an updated recall of Great Value apple juice sold at Walmart amid arsenic concerns, giving the recall a more urgent classification on Friday. The ...
An FDA warning letter is an official message from the United States Food and Drug Administration (FDA) to a manufacturer or other organization that has violated some rule in a federally regulated activity. ... a correspondence that notifies regulated industry about violations that FDA has documented during its inspections or investigations.
A product recall is a request from a manufacturer to return a product after the discovery of safety issues or product defects that might endanger the consumer or put the maker or seller at risk of legal action. Product recalls are one of a number of corrective actions that can be taken for products that are deemed to be unsafe.
A product safety recall happens when a consumer watch group or a manufacturer finds problems with a product. Lots of items can be recalled. Some products that are commonly recalled include: Food ...
Meridia was recalled from the U.S. market in 2010 after it was found to increase a person's risk of heart attack and stroke. Is mislabeled or packaged poorly. Sometimes a medicine is recalled ...
2009–2011 Toyota vehicle recalls. Two of the vehicles under recall: the Toyota Camry (XV40) at top, and the Toyota Corolla (E140) at bottom. The 2009–11 Toyota vehicle recalls involved three separate but related recalls of automobiles by the Japanese manufacturer Toyota Motor Corporation, which occurred at the end of 2009 and the start of 2010.
The ability to recall or unsend an email is not available in AOL Mail, because we provide a web-based service which sends messages instantly and once you send an email message, it's gone from your email server and out of our control. If you're unsure about sending an email, save the message to think things over, then send it later. Feedback.
Recall information. FDA develops a strategy for each individual recall that sets forth how extensively it will check on a company's performance in recalling the product in question. For a Class I recall, for example, FDA would check to make sure that each defective product has been recalled or reconditioned. In contrast, for a Class III recall ...