Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
IBU (ibuprofen) 600 mg tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Tablet/Capsule Specifications
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
IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05
Quantity: 3416 botttles
Why Was This Recalled?
Failed Tablet/Capsule Specifications
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