Hospira Inc. recalls 0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 10 mL, Single-Dose Vial, NDC 0409-9045-01, Hospira, Inc., Lake Fore

Recalled October 16, 2013 · FDA recall D-66295-001 · Hospira

Hazard

Lack of Assurance of Sterility; potential for vial breakage · FDA Class II

Units

187,150 vials

Sold at

Nationwide and Guam and Abu Dhabi

Description

Lack of Assurance of Sterility; potential for vial breakage

Product

0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 10 mL, Single-Dose Vial, NDC 0409-9045-01, Hospira, Inc., Lake Forest, IL 60045

Manufacturer(s)

Hospira Inc.

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