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: Out-of-Specification results were observed for...
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: 4,212 (30-count blister pack)
Why Was This Recalled?
Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 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