Reported Feb 7, 2018 · Terminated
PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC…
PD-Rx Pharmaceuticals, 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: PD-Rx Pharmaceuticals, Inc. · 727 N Ann Arbor Ave · Oklahoma City, OK · 73127-5822
Is this the product you have?
- PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC 55289-673-30; c) 50 tablets NDC 55289-673-50; d) 60 tablets NDC 55289-673-60
- Lot codes and dates
13 of 13 products
Products covered by this recall # Product as published 1 K16E92 Exp. 5/31/18 2 B17A87 Exp. 5/31/18 3 E17A51 Exp. 5/31/18 4 L16B59 Exp. 1/31/18 5 K16E01 Exp. 5/31/18 6 A17F21 Exp. 5/31/18 7 B17D71 Exp. 5/31/18 8 D17E92 Exp. 5/31/18 9 J16D13 Exp. 1/31/18 10 A17D63 Exp. 5/31/18 11 E17A18 Exp. 5/31/18 12 F17B87 Exp. 5/31/18 13 C17C58 Exp. 5/31/18 - Amount recalled
- 7174 bottles
Where it was sold
- Nationwide
Why it was recalled
CGMP deviations.
This product could cause temporary or reversible health problems — stop using it.
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