Dr. Reddy's recalls 400mg Ibuprofen tablets (Rx only) due to impurities exceeding safety limits. Affected lots have specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Dr. Reddy's is recalling 400mg Ibuprofen tablets (Rx only) because tests found impurities at levels above the safety limit. This could pose a risk to health if taken as directed.
The tablets contain impurities that exceed the 0.10% safety limit, with test results showing 0.13% and 0.11%. This could potentially cause health issues if taken as directed, though the exact risk is not specified.
People who have the recalled 400mg Ibuprofen tablets (Rx only) from Dr. Reddy's Laboratories in the US. Those with medical conditions requiring ibuprofen may be at higher risk.
Check for NDC numbers 55111-682-01 (100 tablets) or 55111-682-05 (500 tablets). The affected lots have specific expiration dates and manufacturing codes listed in the recall notice.
Look for NDC numbers 55111-682-01 or 55111-682-05 on the tablet packaging.
The tablets contain impurities that exceed the 0.10% safety limit, as found in testing.
The recall notice does not specify a remedy, so contact Dr. Reddy's Laboratories for further instructions.
Yes, the affected lots have expiration dates up to November 30, 2026.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0646-2024 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0646-2024 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
