Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Subpotent Drug: Subpotent atorvastatin.
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
Amlodipine besylate and Atorvastatin calcium Tablets, 10 mg/20 mg, Packaged in a) 30 Count Bottles (NDC: 43598-318-30) and b) 90 Count Bottles (NDC: 43598-318-90), Rx Only. Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 India
Quantity: a) 16,080 and b) 480 Bottles
Why Was This Recalled?
Subpotent Drug: Subpotent atorvastatin.
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