Temination of FDA Recall

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FDA, eye drop and recall

St. Louis firm recalls more than 75K cases of eye drop products. What to know

A St. Louis firm has issued a voluntary recall for more than 75,000 cases of eye drop products, stating there was a manufacturing deviation that could cause harm, according to the U.S. Food and Drug Administration.

· 1d · on MSN

· 10h

AvKare recalls over-the-counter eye drops after FDA audit

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More than 70,000 eye care products recalled nationwide following FDA audit. What to know

More than 75K cases of eye drops recalled over safety concerns

More than 75,000 cases of eye drops have been recalled in the United States, according to a new report.

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· 1d

Eye drops, solution recalled, products sold nationwide: See list of products

Putnam Daily Voice · 1d

Eye Drops May Be Contaminated, Sparking Recall Of 1.8M+ Bottles

3don MSN

Sandwich Recall Issued as FDA Warns of Possible 'Fatal Infections'

Listeria monocytogenes can be especially dangerous for pregnant women, newborns, older adults and those with weak immune systems.

as.com3d

FDA warning: These popular eye drops could be dangerous. What do I do if I have one of the contaminated lots?

AVKare, a pharmaceutical distributor, released a statement announcing that BRS Analytical Services had issued a voluntary recall after an FDA audit. The recall covers a variety of eye-related ...

al.com10d

FDA sets highest risk level for burger recall

A recall of seafood burgers has been updated to the highest risk by the U.S. Food and Drug Administration. Connecticut-based company Caraluzzi’s Markets initiated the recall in April because its ...

Yahoo4d

FDA: Recall of Ready-to-Eat foods sold in WA for Listeria outbreak, 10 hospitalized in CA, NV

You should contact your healthcare provider right away if you have symptoms of a Listeria infection. For more information on the recall, visit fda.gov.

The Hour3d

Eye drops, other eye care products recalled nationwide over sterility concerns, FDA says

According to the report, on May 6, the FDA classified the recall as "Class II," which indicates "a situation in which use of, or exposure to, a violative product may cause temporary or medically ...

USA Today4d

Artificial tears, other eye products recalled; consumers urged to discontinue use

Pharmaceutical distributor AvKARE was notified of the consumer level drug recall by the recalling firm, BRS Analytical Services LLC. The recall was issued for several products as a result of ...

Mundo Deportivo8d

FDA recalls bean brand over presence of potentially life-threatening ingredient

The U.S. Food and Drug Administration (FDA) has announced the recall of 4,515 cases of 15-ounce (425-gram) cans of Yellowstone Brown Sugar Molasses Baked Beans due to the presence of undeclared ...