Hospira Inc. recalls Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., La
Recalled April 16, 2014 · FDA recall D-1226-2014 · Hospira
Hazard
Labeling; Missing label; ampoules are missing the immediate container label · FDA Class III
Units
237,850 ampoules
Sold at
Nationwide
Description
Labeling; Missing label; ampoules are missing the immediate container label
Product
Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →