Hospira Inc. recalls KETOROLAC Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Fill Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Fores
Recalled April 15, 2015 · FDA recall D-0483-2015 · Hospira
Hazard
Crystallization · FDA Class II
Units
HOSPIRA = 4,339,500 vials. NOVAPLUS = 341,100 vials
Sold at
U.S. Nationwide and International: Guam and Singapore.
Description
Crystallization
Product
KETOROLAC Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Fill Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-3796-01 ---- ALSO labeled under NOVAPLUS label NDC 0409-3796-49
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →