RecallRadar

FDA Drug recall D-1042-2013

IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's Laboratories, Inc., Bridg…

On 2013-09-25 the FDA classified a Class II recall of IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's Laboratories, Inc., Bridg… by Dr Reddy S Laboratories, citing 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.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1042-2013
ClassificationClass II
Statusterminated
Initiated2013-08-29
Published2013-09-25
Last updated2026-09-13 11:51 UTC
CompanyDr Reddy S Laboratories
DistributionUS

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

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.

Identifiers

ndc55111-682-09
ndc55111-682-01
ndc55111-682-05
ndc55111-683-30
ndc55111-683-50
ndc55111-683-09
ndc55111-683-01
ndc55111-683-05
ndc55111-684-30
ndc55111-684-50
ndc55111-684-60
ndc55111-684-09
ndc55111-684-01
ndc55111-684-05
code_infoLot # L300192; Exp. 05/2017

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1042-2013%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.