Hospira Inc. recalls Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Recalled January 9, 2013 · FDA recall D-106-2013 · Hospira
Hazard
Presence of Particulates; may contain glass particles · FDA Class II
Units
361,600/1-mL ampules
Sold at
Nationwide
Description
Presence of Particulates; may contain glass particles
Product
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →