RecallDepth
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.

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

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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