US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 15, 2017 (9 years ago)

Ketorolac Tromethamine Injection, USP 30 mg/mL, packaged in 1 mL single-dose vials, Rx…

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

Why it was recalled

Crystallization: Particulate matter (Ketorolac Calcium Salt) was observed from several lots of retained samples.

What was recalled

Ketorolac Tromethamine Injection, USP 30 mg/mL, packaged in 1 mL single-dose vials, Rx only, Amphastar Pharmaceuticals, Inc., Rancho Cucamonga, CA 91730, NDC 0548-9021-00

Recalling firm
Amphastar Pharmaceuticals, Inc.
NDC code
0548-9021-00
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1124-2017

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.

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