PlainRecalls
FDA Drug Moderate 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.

Reported: September 25, 2013 Initiated: August 29, 2013 #D-1042-2013

Product Description

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.

Details

Units Affected
18852 bottles
Distribution
Nationwide (& Puerto Rico)
Location
Bridgewater, NJ

Frequently Asked Questions

What product was recalled?
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.. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 18852 bottles.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Drug on September 25, 2013. Severity: Moderate. Recall number: D-1042-2013.