Power Stick Deodorant recalled nationwide by FDA
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Rich Ice Cream Co. recalled numerous lots of its products on June 27 over potential contamination with Listeria monocytogenes.
Coffee pods sold nationwide are under recall for a possible health issue, according to notices posted by the company and the U.S. Food & Drug Administration. New Mexico Pinon Coffee is voluntarily recalling lot code 251749 of New Mexico Pinon Coffee Dark Pinon Single Serve Cups in a 10 count box.
Note that some links may require registration or subscription. A New York man who entered an MRI room while a scan was taking place was pulled into the machine by his chain necklace and is now in critical condition. ( CBS News) An Oregon man caught the plague from his cat last year. ( Morbidity and Mortality Weekly Report)
Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.
Sandoz has issued a nationwide recall of two lots of cefazolin for injection due to a labeling error. The mislabeled vials were sent to wholesalers for nationwide distribution. The error was found after a complaint showed that the cefazolin vials were packaged and labeled as penicillin G potassium for injection,
The Food and Drug Administration July 15 announced a recall by Sandoz on certain lots of cefazolin, due to the lots being mislabeled as penicillin G potassium. The FDA said the inadvertent administration of cefazolin following a recommended dosage of penicillin G potassium could pose serious and potentially life-threatening health consequences.
The U.S. Food and Drug Administration raised concerns over ink printing potentially running when exposed to high temperatures.
FDA recalls Dexcom glucose monitors (G6, G7, ONE models) due to alert issues posing severe health risks. Read more here.
The Centers for Disease Control and Prevention and the U.S. the Food and Drug Administration are investigating a Salmonella outbreak in several states linked to recalled frozen sprouted beans.
Class II recalls from the FDA indicate a potential risk to consumer safety where use or exposure to the product may cause temporary or medically reversible adverse health consequences, but serious adverse outcomes are considered unlikely.