Hospira Inc. recalls Gentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gent
Recalled Product
Gentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gentamicin), 2 mL Single-dose Fliptop Vial, (NDC 0409-1207-13), Rx only, Manufactured by Hospira, Inc, Lake Forest, IL 60046 USA.
Hazard / Issue
Presence of Particulate Matter: visible particles were identified floating in the primary container.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot 07-067-DK Exp. 07/13
View official government recall
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