Class II
Terminated
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.
This recall has been terminated (originally issued September 25, 2013).
- Company
- Dr. Reddy'S Laboratories, Inc.
- Recall Initiated
- August 29, 2013
- Posted
- September 25, 2013
- Recall Number
- D-1042-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 18852 bottles
- Firm Location
- Bridgewater, NJ, United States
- Official Source
- View on FDA website ↗
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)
Lot / Code Info
Lot # L300192; Exp. 05/2017
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