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Power Stick Deodorant recalled nationwide by FDA

Explícame on MSN · 55m

FDA Recalls More Than 67,000 Power Stick Deodorants Due to Flaws in the Manufacturing Process

More than 67,000 boxes of Power Stick deodorants have been recalled in the United States due to manufacturing irregularities. The FDA has identified that these products do not meet quality standards,

People on MSN · 2h

FDA Recalls More Than 67,000 Cases of Deodorant

More than 67,000 cases of Power Stick deodorants were recalled, the FDA announced The agency typically encourages consumers to stop use and dispose of any recalled items More than 67,000 cases of deodorant have been recalled nationwide due to safety concerns.

USA TODAY on MSN · 8h

More than 67,000 cases of Power Stick deodorant recalled nationwide

More than 67,000 cases of Power Stick deodorants were recalled for deviating from Food and Drug Administration standards.

Salmonella, Sprouted beans and Recall

UPI on MSN · 1h

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.

KIRO 7 News Seattle · 1h

Recall alert: Sprouted beans sold nationwide recalled for potential Salmonella contamination

The Food and Drug Administration has announced the recall of two types of sprouted beans because they may be contaminated with Salmonella. The recall affects frozen Deep Spouted Mat (Moth) and Deep Sprouted Moong. Both came in 16-ounce bags, the FDA said. They were sold nationwide.

USA TODAY on MSN · 2h

Frozen sprouted beans linked to salmonella outbreak recalled

Health officials have recalled a batch of frozen sprouted beans linked to a salmonella outbreak that has spread across 10 states.

3h

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 ...

9hon 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.

American Hospital Association3h

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 ...

2hon MSN

Southwestern roaster recalls coffee pods due to defect that causes ink to bleed during brewing

One of New Mexico’s largest coffee roasters is recalling some of its single-serve Keurig cups due to a defect that can cause ...

4hon MSN

FDA announces recall of certain Dexcom glucose monitoring devices

FDA recalls Dexcom glucose monitors (G6, G7, ONE models) due to alert issues posing severe health risks. Read more here.

3hon MSN

Company issues nationwide fish recall due to botulism poisoning risk

New York-based Krasniy Oktyabr Inc. USA is recalling a fish product due to the potential risk of botulism poisoning.

6don 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 ...

13h

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 ...

1d

A new recall of injected penicillin may put gains against syphilis in peril

Drugmaker Pfizer is warning doctors that it expects to run low on supplies of Bicillin L-A, a long-acting injection of the ...

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