US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 29, 2021 (5 years ago)

Idarubicin Hydrochloride Injection 20 mg/20 mL

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

Why it was recalled

Lack of Assurance of Sterility

What was recalled

Idarubicin Hydrochloride Injection 20 mg/20 mL, 20 mL single-dose vial, Rx only, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0703-4156-11

Recalling firm
Teva Pharmaceuticals USA
NDC code
0703-4156-11
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0734-2021

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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