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eye drop, recall

USA TODAY on MSN · 21h

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

Over-the-counter ophthalmic products were voluntarily recalled due to a manufacturing deviation discovered during a U.S. Food and Drug Administration audit, a notice says.

TODAY on MSN · 5h

More than 75,000 cases of eye care products recalled, FDA enforcement report says

The pharmaceutical testing lab BRS Analytical Service recalled products used to relieve dry and irritated eyes after "deviations" were found in adhering to FDA safety regulations.

Houston Chronicle on MSN · 4h

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.

Daily Voice on MSN10h

AvKARE Recalls 1.8M+ Eye Drop Bottles After FDA Audit

More than 1.8 million eye drop bottles distributed nationwide are being recalled because the products may not be sterile.

Recall notice: Several types of eyedrops sold nationwide may not be sterile

The issue was discovered during an audit by the FDA and impacts certain eyedrops sold between May 2023 and April 2025.

1d

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

Do you use eye drops? This distributor has announced a voluntary recall covering products sold between 2023 and 2025.

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