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

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

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

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

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

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

Tens of thousands of cases of eye drops have been recalled by BRS Analytical Services. The recall was initiated on April 23, ...

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

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 ...

A nationwide recall has been issued for a number of eye care products in the U.S. as officials urged people to stop using them "immediately." ...

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

BRS Analytical Services, LLC, a pharmaceutical testing laboratory, had issued a nationwide recall on April 23 to over-the-counter ophthalmic products.