Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Excipient Specifications; product manufactured using an excipient...
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
Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 count (NDC 43598-742-90) and b) 1000 count (NDC 43598-742-10) 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, , packaged in bottles.
Quantity: a) 776 bottles, b) 84 bottles
Why Was This Recalled?
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
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