Reported Jan 13, 2016 · Terminated
Azithromycin 500 mg tablets, Rx Only, packaged in a) 1 count, b) 2 count, c) 3 count, and d) 7 count bottles, Packaged…
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?
Azithromycin 500 mg tablets, Rx Only, packaged in a) 1 count, b) 2 count, c) 3 count, and d) 7 count bottles, Packaged by
4 of 4 products
| # | Product as published |
|---|---|
| 1 | 55289-274-79 |
| 2 | 55289-274-02 |
| 3 | 55289-274-03 |
| 4 | 55289-274-07. |
- Lot codes and dates
Lot #s: J12C03J12D19Exp 10/14L12B52L12E79L12G92Exp 12/14A13G14A13H49Exp 01/15B13G53Exp 02/15D13A66Exp 04/15E13E35Exp 05/15F13A58F13D85F13F17F13F27Exp 06/15G13D37G13E57Exp 07/15H13A65H13A74H13C13H13G01Exp 08/15I13C02I13G98Exp 09/15J13C53J13G90Exp 10/15K13A65K13B73K13C98K13E61Exp 11/15L13C59L13F49A14C27A14D09A14F11Exp 12/15
- Amount recalled
- 17,533 bottles
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
cGMP Deviations: This recall is a result of the original manufacturer's recall, in which the firm did not adequately investigate customer complaints.
This product could cause temporary or reversible health problems — stop using it.
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