Apotex Inc. recalls Losartan potassium tablets USP, 25 mg, 90- count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T
Recalled July 15, 2015 · FDA recall D-1212-2015 · Apotex
Hazard
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification. · FDA Class II
Units
45,708 bottles
Sold at
Nationwide, Hawaii and Puerto Rico
Description
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Product
Losartan potassium tablets USP, 25 mg, 90- count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private Limited, Plot 1 & 2, Bommasandra Industrial Area, 4th Phase Jigani Link Road, Bangalore, Karnataka, 560099, India NDC 60505-3160-9
Manufacturer(s)
Apotex Inc.
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →