Over-the-counter ophthalmic products were voluntarily recalled due to a manufacturing deviation discovered during a U.S. Food ...

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

The pharmaceutical testing lab BRS Analytical Service recalled products used to relieve dry and irritated eyes after ...

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

The FDA recalled eye drops, which were intended to soothe dry, itchy eyes, because of a “lack of assurance of sterility.” ...

More than 76,000 eye drops and other eye care products are being voluntarily recalled after an audit by the Food and Drug ...

Over 75,000 bottles of eye drops have been recalled due to FDA audit findings of manufacturing violations, including ...

Nearly 76,000 cases of eye drops have been recalled nationwide by BRS Analytical Services, a pharmaceutical consulting firm, according to an FDA enforcement report.

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

More than 70,000 cases of ophthalmic products are being recalled for manufacturing deviations, according to a press release by distributor AvKARE. The recalled products, which include eye drops and ...

The products in question were shipped out up until recently. The distributor recommends that further use of the products ...

A pharmaceutical distributor issued an urgent notice about a voluntary recall for five over-the-counter eye care products ...