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Company recalls 67,000 cases of stick deodorant
WASHINGTON - A.P. Deauville, LLC, has voluntarily recalled more than 67,000 cases of various Power Stick roll-on antiperspirant deodorants nationwide due to deviations from current Good Manufacturing Practice regulations, according to an enforcement report of the Food and Drug Administration.
Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.
MedPage Today on MSN15h
Gain-of-Function Research Halted; Antibiotic Recall; FDA Revokes 52 Food StandardsWhite House officials overrode NIH career staff in deciding which "dangerous gain-of-function research" projects on viruses ...
Consumers who have purchased the affected product should not consume it, per the FDA. For information on refunds (or for more ...
The Food and Drug Administration has announced the recall of two types of sprouted beans because they may be contaminated ...
As such, the FDA has classified the New Mexico Pinon Coffee pod recall as a Class III risk. The FDA defines such a risk as “a ...
New York-based Krasniy Oktyabr Inc. USA is recalling a fish product after it was found by inspectors to be uneviscerated, posing a risk of botulism poisoning.
The move is expected to cause a “near-term stock out of Bicillin L-A,” Pfizer said in its statement, with the drugmaker now ...
Class II recalls from the FDA indicate a potential risk to consumer safety where use or exposure to the product may cause ...
The Food and Drug Administration (FDA) upgraded a blueberry recall this week to the highest risk level amid concerns of ...
YoCrunch yogurt products are being recalled nationwide by manufacturer Danone U.S., the U.S. Food and Drug Administration ...
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