Aurolife Pharma, LLC recalls Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53); b)
Recalled September 25, 2019 · FDA recall D-1865-2019 · Aurolife Pharma
Hazard
Failed Impurities/Degradation Specifications · FDA Class II
Units
a) 9662 cartons; b) 7382 cartons; c) 5184 cartons; d) 9842 cartons
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications
Product
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.
Manufacturer(s)
Aurolife Pharma, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →