Class II
Terminated
Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira, Inc., Lake Forest, IL 60045, USA. NDC carton: 0409-3506-01; NDC vial: 0409-3506-11
- Company
- Pfizer Inc.
- Recall Initiated
- September 20, 2018
- Posted
- October 31, 2018
- Recall Number
- D-0095-2019
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 71,075 vials
- Firm Location
- New York, NY, United States
Reason for Recall
Lack of assurance of sterility: loss of container integrity.
Distribution
Nationwide in the US and Puerto Rico
Lot / Code Info
Lot: 609G047, EXP 10/2018
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