Reported Sep 25, 2013 · Terminated
IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Distributed by Dr. Reddy's…
Dr. Reddy's Laboratories, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Dr. Reddy's Laboratories, Inc. · 200 Somerset Corporate Blvd Fl 7th · Bridgewater, NJ · 08807-2862
Is this the product you have?
- 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.
- Lot codes and dates
Lot # L300192Exp. 05/2017
- Amount recalled
- 18852 bottles
Where it was sold
- Nationwide
- PR
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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