Nationwide recall affects five types of dry eye treatments due to manufacturing violations and sterility concerns.

Pharmaceutical company AvKare has issued a voluntary recall on several of its over-the-counter products for dry and irritated eyes, citing regulatory "deviations" identified during an audit by the ...

Several types of eye drops sold nationwide have been recalled due a manufacturing issue which can cause a health hazard ...

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.

Five different eye drop products that were sold between May 2023 and April 2025 were identified in a recall from manufacturer AvKARE.

Millions of cartons of eye drops and other eye products have been recalled nationwide due to manufacturing and quality issues ...

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

Thousands of cases of ophthalmic products were voluntarily recalled after a manufacturing deviation identified during an inspection from the FDA.

Lubricant Eye Drops Solution; national drug code (NDC): 50268-126-15; 32,876 cases of Carboxymethylcellulose Sodium ...

They're trusted for relieving a specific type of eye discomfort, but there's an "unknown" potential health hazard if using ...

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

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