November 2018 FDA Recall Clopidogrel Bisulfate by Dr. Reddy's Laboratories, Inc.
D-0283-2019 - Failed Dissolution Specification

This Class II drug recall was voluntarily initiated by Dr. Reddy's Laboratories, Inc. on November 7, 2018 for the product Clopidogrel Bisulfate. The FDA reported the reason for recall as failed dissolution specification. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0283-2019

Reason for Recall
Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.
Initiated
11-07-2018
Reported
11-28-2018
Quantity
4,212 (30-count blister pack)

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Dr. Reddy's Laboratories, Inc.
Clopidogrel Tablets, USP, 300 mg, 30 (5 x 6 unit-dose) count blister pack, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Srikakulam - 532 409, India, NDC 55111-671-31

Batch or Lot Expiration Information

Lot# : T600530, Exp 11/18