The five recalled products include lubricant eye drops and eye gels, which consumers should immediately cease using, AvKare warned. The items affected were shipped May 26, 2023 through April 21, 2025.

However, there have already been several eye drop products recalled across the country just this year. A few weeks ago, over 1.8 million eye drops apparently used to relieve dry eye symptoms were ...

Several types of eye drops sold nationwide have been recalled due a “manufacturing” issue which can cause a health hazard. AvKARE, the distributor of the eye drops, posted the recall on its ...

Lubricant Eye Drops Solution (NDC# 50268-126-15) Polyvinyl Alcohol Ophthalmic Solution (NDC# 50268-678-15) A full list of lot codes and specific expiration dates can be found here.

NDC# 50268-126-15 Lubricant Eye Drops Solution; recall number D-0407-2025 NDC# 50268-678-15 Polyvinyl Alcohol Ophthalmic Solution; recall number D-0408-2025 Detailed lots numbers and specific ...

NDC #50268-126-15 Lubricant Eye Drops Solution NDC #50268-678-15 Polyvinyl Alcohol Ophthalmic Solution The recalled products were shipped out May 2023 through April 2025, and have expiration dates ...

14,333 cases of Polyvinyl Alcohol Ophthalmic Solution 1.4%, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle; Where were the products distributed?

A n urgent nationwide recall has been issued for over 1.8 million cartons of eye drops due to potential sterility issues that could lead to serious eye infections, vision loss, or even blindness ...

The eye drops and solutions were shipped between May 26, 2023 and April 21, 2025. Recalled products include: • 13,104 cases of Lubricant Eye Drops Solution; national drug code NDC 50268-126-15 ...

WASHINGTON — Thousands of eye care products, including lubricant eye drops and artificial tears, have been voluntarily recalled due to a "manufacturing deviation" found following a U.S. Food and ...

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 ...