Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment Recalled by Allergan Sales, LLC Due to Failed Impurities/Degradation Specifications: stability testing results did not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Allergan Sales, LLC directly.
Affected Products
Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile, 3.5 g tube, RX only, Manufactured by Allergan, Irvine, California, 92612, U.S.A., NDC: 0023-0313-04.
Quantity: 648 units
Why Was This Recalled?
Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Allergan Sales, LLC
Allergan Sales, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report