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eye drop, 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.

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

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

Thousands of eye care products sold nationwide are being recalled: See the list of impacted items

Nearly 76,000 cases of eye care products have been voluntarily recalled by their manufacturer following an audit by the U.S. Food and Drug Administration.

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Voluntary recall issued for eye drops, eye care products sold nationwide

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Eye care products recalled across US; people urged to stop using ‘immediately'

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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. AvKARE issued the voluntary recall for 1,819,080 cartons of eye drops in 75,795 cases.

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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.

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Over 75,000 Eye Drop Bottles Recalled After FDA Audit. Check Full List Here

Over 75,000 bottles of eye drops have been recalled due to FDA audit findings of manufacturing violations, including sterility concerns. AvKare, the manufacturer of the affected products, stated the health risks are "unknown" but urged consumers to discontinue use.

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.

Avkare eyedrops recalled for "manufacturing deviations"

Avkare has recalled a range of its lubricating eye drops for what the company said are "manufacturing deviations."