PlainRecalls
FDA Drug Moderate Class II Terminated

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.

Reported: July 17, 2013 Initiated: May 2, 2013 #D-686-2013

Product Description

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.

Reason for Recall

Presence of Particulate Matter: visible particles were identified floating in the primary container.

Details

Recalling Firm
Hospira Inc.
Units Affected
168,300 vals
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
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.. Recalled by Hospira Inc.. Units affected: 168,300 vals.
Why was this product recalled?
Presence of Particulate Matter: visible particles were identified floating in the primary container.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 17, 2013. Severity: Moderate. Recall number: D-686-2013.