# FDA recall D-1042-2013

> **Dr. Reddy's Laboratories, Inc.** · Class II · drug recall initiated 2013-08-29.

## 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.

## Distribution

Nationwide (& Puerto Rico)

## Key facts

- **Recall number:** D-1042-2013
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-08-29
- **Report date:** 2013-09-25
- **Termination date:** 2014-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bridgewater, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1042-2013

## Citation

> AI Analytics. FDA recall D-1042-2013. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1042-2013. Source: US FDA. Licensed CC0.

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