Class II
Terminated
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
- Company
- Hospira Inc., A Pfizer Company
- Recall Initiated
- February 10, 2017
- Posted
- March 1, 2017
- Recall Number
- D-0480-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 578,784 bags
- Firm Location
- Lake Forest, IL, United States
Reason for Recall
Lack of Sterility Assurance: customer report of leaking bag
Distribution
Nationwide and Puerto Rico
Lot / Code Info
Lot: 54-054-JT, 6/1/2017
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