Drug recall D-926-2013
Product
Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01
Reason for recall
Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop vials.
Lots and codes
Lot 25048DK Exp. 01/15
Recall details
- Recalling firm
- Hospira, Inc., Lake Forest, IL
- Quantity
- 345,800 vials
- Distribution
- Naitonwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 12, 2013
- Terminated
- October 28, 2014
Related products
- Ketorolac Tromethamine – drug information
- NDC 0409-3795 Ketorolac Tromethamine · Ketorolac Tromethamine 30 mg/mL · Hospira, Inc.
- NDC 0409-3793 Ketorolac Tromethamine · Ketorolac Tromethamine 15 mg/mL · Hospira, Inc.
- NDC 0409-3796 Ketorolac Tromethamine · Ketorolac Tromethamine 60 mg/2mL · Hospira, Inc.