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FDA recalls over 67,000 cases of Power Stick deodorant. See where products were sold
The manufacturer announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good ...
FDA issues risk warning for nationwide cough syrup recall
Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.
Coffee pods recall triggers lowest-risk warning from FDA
A production issue raised concerns that ink printing on some cups could run when exposed to high temperatures, inspectors ...
FDA Recalls More Than 67,000 Cases of Deodorant
Various Power Stick deodorants have been recalled due to "Current Good Manufacturing Practice deviations", according to the U ...
Nationwide Sausage Recall as Consumer Warning Issued
Kayem Foods Inc. has issued a voluntary recall for more than 24,000 pounds of its Sweet Apple Chicken Sausages.
The FDA Announces Recall on Bread Sold at Walmart and Kroger in These States
Lewis Bake Shop is issuing a voluntary recall on their Artisanal Style 1/2 Loaf, which contains undisclosed hazelnuts — a ...
FDA Announces Massive Deodorant Recall—Here's What to Look For
Check the label on your deodorant ASAP. Tens of thousands of cases of Power Stick antiperspirant deodorant have been recalled ...
FDA Issues Risk Warning for Potato Chips Recall
A recall of potato chips due to the possible presence of an undeclared allergen has been issued the second-highest risk warning by the U.S. Food and Drug Administration ( FDA ). Saratoga Potato Chips ...
Deodorant recall: More than 67,000 cases sold at Walmart, Dollar Tree, Amazon
More than 67,000 cases of deodorant sold at major retailers are being recalled due to a manufacturing issue. According to a ...
FDA Recalls Popular Yogurt Products Nationwide Over ‘Choking’ Hazard
Consumers who have purchased the affected product should not consume it, per the FDA. For information on refunds (or for more ...
FDA updates recall of certain Dexcom CGM speakers
FDA recalls Dexcom glucose monitors (G6, G7, ONE models) due to alert issues posing severe health risks. Read more here.
American Hospital Association1 天
FDA announces recall of cefazolin by Sandoz for mislabeling
The Food and Drug Administration July 15 announced a recall by Sandoz on certain lots of cefazolin, due to the lots being ...