FDAFDA · Food and drugs·Recall number D-926-2013
Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01
Published September 4, 2013 · Recall initiated: August 12, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop vials.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- KETOROLAC TROMETHAMINE
- Manufacturer
- Hospira, Inc.
- Distributor
- Naitonwide
- Lot
- Lot 25048DK Exp. 01/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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