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

The FDA's website also lists the number of cases involved in the recall: 13,104 cases of Lubricant Eye Drops Solution ...

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.

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

Several eye care products, including artificial tears and gel drops, are being recalled due to a manufacturing error that may cause a “health hazard,” according to the U.S. Food and Drug ...

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

If you have recalled eye drops, AvKare’s instructions are to fill out its recall form with the quantity of affected products in your possession and fax the form to 931-292-6229 or send it via ...

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

Pharmaceutical distributor AvKARE was notified of the consumer level drug recall by the recalling firm, BRS Analytical Services LLC. The recall was issued for several products as a result of ...

Ophthalmic products were voluntarily recalled due to a manufacturing deviation discovered during an FDA audit. See the list of products here.

The product recall effects five different dry eye drop products manufactured by AvKARE that were sold between May 2023 and April 2025. The Tennessee-based pharmaceutical company said the audit ...