Reported Sep 4, 2013 · Terminated
Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01
Hospira, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira, Inc. · 600 N Field Dr Bldg J45 · Lake Forest, IL · 60045
Is this the product you have?
- Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01
- Lot codes and dates
- Lot 25048DK Exp. 01/15
- Amount recalled
- 345,800 vials
Why it was recalled
Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop vials.
This product could cause temporary or reversible health problems — stop using it.
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