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Bloodshot red eye revealing subconjunctival hemorrhage and conjunctival inflammation, signaling potential ocular infection or irritation
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A major eye care product recall has been issued across the U.S., affecting tens of thousands of units.

Here’s a breakdown of what’s happening, why it matters, what steps you should take, and which products to look for.

Why This Recall Matters

  • Over 70,000 units recalled: The FDA issued a Class II recall, meaning the products could pose temporary or reversible health risks.
  • Manufacturing issues: BRS Analytical Service, LLC initiated the voluntary recall after failing to meet FDA’s Current Good Manufacturing Practices (cGMP) standards.
  • Potential risks: No confirmed health issues have been reported, but the quality of the products cannot be guaranteed.

What You Need to Know

  • The U.S. FDA discovered deviations during an inspection, prompting immediate action.
  • The recalled products may not be sterile or safe for use in or around the eyes.
  • Distributed by AvKARE, the affected products were available between May 26, 2023, and April 21, 2025.

Full List of Recalled Eye Care Products

Product NameNDC Number
Artificial Tears Ophthalmic Solution50268-043-15
Carboxymethylcellulose Sodium Ophthalmic Gel 1%50268-066-15
Carboxymethylcellulose Sodium Ophthalmic Solution50268-068-15
Lubricant Eye Drops Solution50268-126-15
Polyvinyl Alcohol Ophthalmic Solution50268-678-15

What To Do If You Have These Products

  1. Stop using them immediately.
  2. Check the NDC numbers on the packaging (see list above).
  3. Return the products for a full refund, including shipping costs.
  4. Contact AvKARE with questions or to initiate a return.
  5. Monitor for symptoms like eye irritation, redness, or pain—and consult a healthcare provider if concerned.

Who to Contact

AvKARE has pledged to assist consumers and provide full credit. If you have questions:

  • Visit AvKARE’s website for their official recall notice and return instructions
  • Contact their customer service via the number or form listed on their recall page