Hospira Inc. recalls KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Fore
Recalled April 15, 2015 · FDA recall D-0482-2015 · Hospira
Hazard
Crystallization · FDA Class II
Units
HOSPIRA = 13,720,475 vials, NOVAPLUS = 1,528,500 vials
Sold at
U.S. Nationwide and International: Guam and Singapore.
Description
Crystallization
Product
KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-3795-01 --- Also labeled under NOVAPLUS label NDC 0409-3795-49
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →