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Class IIOngoing

Polyvinyl Alcohol Ophthalmic Solution 1.4% recall

FDA recall D-0408-2025 · initiated Apr 23, 2025

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated May 14, 2025How we research

BRS Analytical Services, LLC recalled Polyvinyl Alcohol Ophthalmic Solution 1.4% in Apr 2025 — an FDA Class II recall (D-0408-2025) because cGMP deviations and lack of assurance of sterility.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

cGMP deviations and lack of assurance of sterility.

Sterility could not be assured

The maker could not guarantee the product was sterile. That matters most for injections and eye products, where a contaminated dose reaches past the body's defences.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot, expiry: Lot 120, exp 10/02/25; Lot 122, exp 10/09/25; Lot 123, exp 10/12/25; Lot 124, exp 10/16/25; Lot 138, exp 1/08/26; Lot 142, exp 1/29/26; Lot 143, exp 2/01/26; Lot 144, exp 2/07/26; Lot 145, exp 2/12/26; Lot 146, exp 2/15/26; Lot 147, exp 2/21/26; Lot 148, exp 2/27/26; Lot 149, exp 3/04/26; Lot 150, exp 3/11/26; Lot 158, exp 4/15/26; Lot 159, exp 4/22/26; Lot 176, exp 7/24/26; Lot 177, exp 7/28/26; Lot 178, exp 7/31/26; Lot 179, exp 8/05/26.

Quantity recalled: 14,333 cases (24 cartons per case)

Details

Product
Polyvinyl Alcohol Ophthalmic Solution 1.4%, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-678-15.
Recalling company
BRS Analytical Services, LLC
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide in the USA
Initiated
Apr 23, 2025
FDA report date
May 14, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Polyvinyl Alcohol Ophthalmic Solution 1.4% recalled?
BRS Analytical Services, LLC recalled Polyvinyl Alcohol Ophthalmic Solution 1.4% in Apr 2025 — an FDA Class II recall (D-0408-2025) because cGMP deviations and lack of assurance of sterility. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Polyvinyl Alcohol Ophthalmic Solution 1.4% recalled?
Per the FDA enforcement record, the reason for recall D-0408-2025 was: cGMP deviations and lack of assurance of sterility.
Is a recalled Polyvinyl Alcohol Ophthalmic Solution 1.4% dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Polyvinyl Alcohol Ophthalmic Solution 1.4% are affected?
Distributed: Nationwide in the USA. The recall covers these lots — Lot, expiry: Lot 120, exp 10/02/25; Lot 122, exp 10/09/25; Lot 123, exp 10/12/25; Lot 124, exp 10/16/25; Lot 138, exp 1/08/26; Lot 142, exp 1/29/26; Lot 143, exp 2/01/26; Lot 144, exp 2/07/26; Lot 145, exp 2/12/26; Lot 146, exp 2/15/26; Lot 147, exp 2/21/26; Lot 148, exp 2/27/26; Lot 149, exp 3/04/26; Lot 150, exp 3/11…. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0408-2025.

Source: openFDA Drug Enforcement record D-0408-2025

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