Nearly 76,000 cases of eye care products – including eye drops sold nationwide – have been recalled by their manufacturer.

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

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

Several eye drop products are being voluntarily recalled due to manufacturing issues that may pose a potential health risk.

The FDA's website also lists the number of cases involved in the recall: 13,104 cases of Lubricant Eye Drops Solution (National Drug Code: 50268-126-15) The recalled items were first shipped between ...

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

The recall alert involves BRS Analytical Services and products sold across the country. Officials said the recall is over manufacturing concerns and cannot rule out patient risks from using these ...

More than 1.8 million cartons of eye drops have been recalled nationwide due to manufacturing issues that may have made the products unsterile. Recall notices from the distributor, AvKARE ...

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. Pharmaceutical ...

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

An eye drop manufacturer has announced a voluntary recall of certain dry eye drops after an audit from the U.S. Food and Drug Administration found "manufacturing cGMP deviations," and has advised ...

If you use eye drops, you need to be aware of this important voluntary recall from BRS Analytical Service, LLC. The recall ...