Hospira Inc. recalls 5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 6004
Recalled October 9, 2013 · FDA recall D-66201-001 · Hospira
Hazard
Presence of Particulate Matter; report of visible particulates in the glass ampule · FDA Class II
Units
86,400 ampuls
Sold at
Nationwide
Description
Presence of Particulate Matter; report of visible particulates in the glass ampule
Product
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →