US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 6, 2014 (12 years ago)

Ketorolac Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Single-dose Fliptop Vial…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.

What was recalled

Ketorolac Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Single-dose Fliptop Vial, packaged in 25 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-3796-01.

Recalling firm
Hospira Inc.
NDC code
0409-3796-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0388-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Ketorolac recalls

See all