FDAFDA · Food and drugs·Recall number D-1057-2017
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Published August 9, 2017 · Recall initiated: July 28, 2017
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
Failed Tablet/Capsule Specification: out of specification for tablet weight.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- PD-Rx Pharmaceuticals, Inc.
- Distributor
- Nationwide
- Lot
- Lot: A17F55 Exp. 06/30/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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