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Walmart, FDA and recall

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.

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

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Deodorant recall: More than 67,000 cases sold at Walmart, Dollar Tree, Amazon

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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.

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

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· 8h

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...

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

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Deodorant sold by Walmart, Amazon recalled nationwide

salmonella, frozen sprouted beans and FDA recalls

Digest more

· 4h · on 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.

· 1d · on MSN

Frozen sprouted beans linked to salmonella outbreak recalled

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CDC warns of salmonella outbreak in frozen beans

10hon MSN

FDA Issues Highest Risk Warning For Dubai Chocolate Recall

The Food and Drug Administration has updated their recall of a batch of Dubai chocolate spread to Class I, their highest level, due to risk of salmonella contamination.

Weaver Nut Company chocolate recall under FDA's highest risk level

The FDA recalled some chocolate products by the Weaver Nut Company chocolate, warning about possible serious to life-threatening allergic reactions.

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.

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.

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.

The Healthy @Reader's Digest3d

FDA: Boar’s Head Deli Brand Has Initiated Another Grocery Recall, This Time Affecting One State

Exactly a year after the brand's historically large lunch meat recall comes a report about an issue with another mainstream product.