Hospira Inc. recalls METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-

Recalled March 27, 2013 · FDA recall D-206-2013 · Hospira

Hazard

Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal. · FDA Class II

Units

567,624 bags

Sold at

Nationwide.

Description

Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal.

Product

METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)

Manufacturer(s)

Hospira Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →