Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 count (NDC 43598-744-30), b) 90 count (NDC 43598-744-9
Recalled November 10, 2021 · FDA recall D-0082-2022 · Dr. Reddy's Laboratories
Hazard
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity · FDA Class II
Units
a) 30,839 bottles, b) 3,830 bottles
Sold at
Nationwide in the US
Description
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Product
Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 count (NDC 43598-744-30), b) 90 count (NDC 43598-744-90) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →