IBU — Class II drug recall D-1042-2013
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2013-09-25, distributed nationwide. Labeling: Incorrect or missing lot and/or exp date- This product is being recalled due to an incorrect expirat
| Recall number | D-1042-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dr. Reddy's Laboratories, Inc., Bridgewater, NJ, United States |
| Recall initiated | 2013-08-29 |
| Classified | 2013-09-13 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2014-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 18,852 bottles |
| Reason classes | labeling |
| NDC | 55111-0682, 55111-0682-01, 55111-0682-05, 55111-0682-09, 55111-0683, 55111-0683-01, 55111-0683-05, 55111-0683-09, 55111-0683-30, 55111-0683-50, 55111-0684, 55111-0684-01, 55111-0684-05, 55111-0684-09, 55111-0684-30, 55111-0684-50, 55111-0684-60 |
| Lot numbers | L300192 |
| Expiration dates | 2017-05 |
Product
IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's Laboratories, Inc., Bridgewater, NJ 08807 USA.
Reason for recall
Labeling: Incorrect or missing lot and/or exp date- This product is being recalled due to an incorrect expiration date of 05/2017. The correct expiration date is 10/2016.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1042-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.