Hospira Inc., A Pfizer Company recalls METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc
Recalled March 1, 2017 · FDA recall D-0480-2017 · Hospira Inc., A Pfizer
Hazard
Lack of Sterility Assurance: customer report of leaking bag · FDA Class II
Units
578,784 bags
Sold at
Nationwide and Puerto Rico
Description
Lack of Sterility Assurance: customer report of leaking bag
Product
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
Manufacturer(s)
Hospira Inc., A Pfizer Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →