Lubricant Eye Drops Moisturizing Twin Pack: 0363-0185-49; lot 19095. Sodium Chloride Ophthalmic Ointment, 5% Hypertonicity Eye Ointment: 0363-7500-50; lot TCI.

The four products being recalled are sold under the brand names Equate, CVS Health and AACE Pharmaceuticals. 1 weather alerts 1 closings/delays. Watch Now. 1 weather alerts 1 closings/delays.

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 ...

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.

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

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 ...

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 ...

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.

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.

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.

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 ...

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 ...