Hospira Inc. recalls Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 6
Recalled November 30, 2016 · FDA recall D-0153-2017 · Hospira
Hazard
Lack of Assurance of Sterility: Complaints of broken tips on the ampules. · FDA Class II
Units
797,800 ampules
Sold at
Nationwide
Description
Lack of Assurance of Sterility: Complaints of broken tips on the ampules.
Product
Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093-32
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →