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 ...

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 ...

A testing lab recalled more than 75,000 cases of eye drop solution after the FDA found deviations from proper manufacturing practices. Here's what to buy instead.

In all, 75,795 cases have been recalled, or 1.8 million cartons of eye drops. The reason for the recall is the potential lack of sterility and cGMP deviations.

The Brief. AvKARE has recalled about 1.8 million cartons of eye drops nationwide after an FDA audit flagged unspecified manufacturing and quality issues.

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 ...

Nearly 76,000 cases of AvKare eye drops have been recalled nationwide. The current health hazard posed to users of the eye drops is unknown, but possible risks cannot be ruled out, AvKare said.

Recalled products include: • 13,104 cases of Lubricant Eye Drops Solution; national drug code NDC 50268-126-15 • 32,876 cases of Carboxymethylcellulose Sodium Ophthalmic Solution; NDC 50268-068-15 ...

Lubricant Eye Drops Solution (NDC# 50268-126-15) Polyvinyl Alcohol Ophthalmic Solution (NDC# 50268-678-15) These products were distributed from May 26, 2023, to April 21, 2025.

Several eye care products, including artificial tears and ophthalmic solutions, are recalled due to quality concerns following an FDA audit. Recalled products include artificial tears, lubricant ...

By the numbers: About 1.8 million cartons of eye drops were recalled, according to the FDA.. What we know: Products subject to the recall include:. NDC# 50268-043-15 Artificial Tears Ophthalmic ...