Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01
Recall Number: D-926-2013
Firm: Hospira, Inc.
Classification: Class II
Status: Terminated
Report Date: 20130904
Initiation Date: 20130812
Termination Date: 20141028
Reason for Recall
Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop vials.
Product Description
Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01