Hospira Inc. recalls Gentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gentamicin), 2 mL Single-dose Fliptop Vial, (NDC 0409-1207-13),
Recalled July 17, 2013 · FDA recall D-686-2013 · Hospira
Hazard
Presence of Particulate Matter: visible particles were identified floating in the primary container. · FDA Class II
Units
168,300 vals
Sold at
Nationwide
Description
Presence of Particulate Matter: visible particles were identified floating in the primary container.
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.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →