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FDA, Deodorant

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.

· 1h

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

· 17h · on MSN

FDA Recalls More Than 67,000 Cases of Deodorant

· 18h

Manufacturer recalls 67,000 cases of popular deodorant brand

More than 67,000 cases of a popular deodorant brand sold by retailers nationwide were recalled due to an undisclosed manufacturing defect.

· 20h

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

· 1d

3hon MSN

FDA Issues Risk Warning for Ice Cream Recalled in 23 States

Rich Ice Cream Co. recalled numerous lots of its products on June 27 over potential contamination with Listeria monocytogenes.

MedPage Today1h

MRI Leaves Man in Critical Condition; Dexcom Recall After 56 Injuries; Drug Denials

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)

Coffee pods recalled for health issue as 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. 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.

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.

19h

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 Association18h

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.

2don MSN

Coffee pods recall triggers lowest-risk warning from FDA

The U.S. Food and Drug Administration raised concerns over ink printing potentially running when exposed to high temperatures.

16hon MSN

Salmonella outbreak prompts public health officials to recall beans

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.