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

Vecuronium Bromide for Injection 10 mg, 10mL vial, Rx only, Teva Pharmaceuticals USA…

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

Vecuronium Bromide for Injection 10 mg, 10mL vial, Rx only, Teva Pharmaceuticals USA, North Wales, PA 19454, NDC 0703-2914-01

Recalling firm
Teva Pharmaceuticals USA
NDC code
0703-2914-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0735-2021

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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