FDAFDA · Food and drugs·Recall number 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., Bridgewater, NJ 08807 USA.
Published September 25, 2013 · Recall initiated: August 29, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- IBU
- Manufacturer
- Dr. Reddy's Laboratories, Inc.
- Distributor
- Nationwide (& Puerto Rico)
- Lot
- Lot # L300192; Exp. 05/2017
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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