Hospira Inc. recalls Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, 50 mL Single-dose Flip top Vial (C-II), Rx only, 25 units per
Recalled December 17, 2014 · FDA recall D-0294-2015 · Hospira
Hazard
Lack of Assurance of Sterility; improperly crimped fliptop vials · FDA Class II
Units
62,650 vials
Sold at
Nationwide
Description
Lack of Assurance of Sterility; improperly crimped fliptop vials
Product
Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, 50 mL Single-dose Flip top Vial (C-II), Rx only, 25 units per box/50 units per case, Hospira Inc., Lake Forest, IL --- NDC 0409-9094-61
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →