Hospira Inc. recalls 0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 50 mL, Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake For
Recalled January 8, 2014 · FDA recall D-395-2014 · Hospira
Hazard
Lack of assurance of sterility; equipment failure led to potential breach in asceptic process. · FDA Class II
Units
65109 vials
Sold at
US Nationwide.
Description
Lack of assurance of sterility; equipment failure led to potential breach in asceptic process.
Product
0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 50 mL, Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045. NDC #0409-9046-01.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →