Hospira Inc. recalls Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, C-II, (50 mcg/mL), 50 mL Single-dose Fliptop Vial, Rx only. H
Recalled July 23, 2014 · FDA recall D-1433-201 · Hospira
Hazard
Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing. · FDA Class II
Units
47,400 vials
Sold at
U.S. Nationwide
Description
Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.
Product
Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, C-II, (50 mcg/mL), 50 mL Single-dose Fliptop Vial, Rx only. Hospira, Inc., Lake Forest, IL 60045. NDC: 0409-9094-61.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →