Hospira Inc. recalls QUELICIN (succinylcholine chloride) Injection, USP, 200 mg (20 mg/mL) 10 mL, Rx only, HOSPIRA, INC. LAKE FOREST, IL 6004
Recalled May 15, 2013 · FDA recall D-315-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial. · FDA Class II
Units
139,200 vials
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Product
QUELICIN (succinylcholine chloride) Injection, USP, 200 mg (20 mg/mL) 10 mL, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, , NDC 0409-6629-02
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →