D-1057-2017 Class II Terminated
FDA drug recall D-1057-2017 was initiated by PD-Rx Pharmaceuticals, Inc. on July 28, 2017 and is designated Class II. Reason for recall: Failed Tablet/Capsule Specification: out of specification for tablet weight. The recall status is terminated (terminated December 6, 2017). Affected quantity: 100 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- August 9, 2017
- Initiation Date
- July 28, 2017
- Termination Date
- December 6, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 100 bottles
Product Description
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Reason for Recall
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Distribution Pattern
Nationwide
Code Information
Lot: A17F55 Exp. 06/30/2018