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Power Stick Deodorant recalled nationwide by FDA

FDA recalls over 67,000 cases of Power Stick deodorant. See where products were sold

Consumers may want to consider finding an alternative deodorant after more than 67,000 cases of Power Stick deodorants were recalled.

· 17h

The FDA Announces Recall on Bread Sold at Walmart and Kroger in These States

· 15h

FDA triggers recall of over 67,000 power stick deodorants | ChicagoNOW

· 13h

Over 67K cases of deodorant sold at Walmart, Amazon have been recalled

Products impacted by the recall include the Power Stick for her roll-on Antiperspirant Deodorant Powder Fresh (1.8 oz/53 mL), the Power Stick Invisible Protection Roll-On Antiperspirant Deodorant Spr...

· 1d

Over 67,000 Cases of This Popular Deodorant Have Been Recalled—Here's What to Know

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Check your deodorant: 67,000 cases of Power Stick deodorant recalled, including in RI

2don MSN

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 said.

The Daily News1h

Coffee pods recalled for health issue; FDA sets risk level

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.

American Hospital Association1d

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 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.

1don MSN

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.

9hon MSN

FDA recalls frozen sprouted beans produced by Sugarland company for links to salmonella outbreak

Health officials have recalled two products produced by Chenak LLC, which has a location in Sugarland, for ties to a salmonella outbreak.

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Food and Drug Administration

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Good manufacturing practice

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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.

7don MSN

FDA Issues Risk Warning for Sunscreen Recall in Multiple States

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.