Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP Recalled by Aurolife Pharma, LLC Due to Failed Impurities/Degradation Specifications
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 Aurolife Pharma, LLC directly.
Affected Products
Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53); b) 30-count cartons (NDC 60000-409-30); c) 45-count bonus cartons (NDC 60000-409-48); d) 45-count cartons (NDC 60000-409-45); CAREone, Distributed by: Foodhold U.S.A., LLC, Landover, MD 20785.
Quantity: a) 9662 cartons; b) 7382 cartons; c) 5184 cartons; d) 9842 cartons
Why Was This Recalled?
Failed Impurities/Degradation Specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aurolife Pharma, LLC
Aurolife Pharma, 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