Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution Specifications; during long term stability testing.
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
Lansoprazole Delayed-Release Capsules, USP, 15 mg, a) 30-count bottle, (NDC 55111-398-30), b) 90-count bottle, (55111-398-90), Rx Only, Manufactured. By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090, India
Quantity: 8,352 bottles (30-count), 1,368 bottles (90-count)
Why Was This Recalled?
Failed Dissolution Specifications; during long term 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