Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Clopidogrel Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed dissolution specification -Two additional lots being recalled...
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 Dr. Reddy's Laboratories, Inc. directly.
Affected Products
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
Quantity: 4,404 (30 count blister packs)
Why Was This Recalled?
Failed dissolution specification -Two additional lots being recalled due to Out-of-Specification results observed for dissolution at 18th month stability testing.
Where Was This Sold?
Product was distributed to 4 major distributors who distributed the product throughout the United States.
About Dr. Reddy's Laboratories, Inc.
Dr. Reddy's Laboratories, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report