US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 7, 2024 (3 years ago)

Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx…

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

Why it was recalled

cGMP Deviations: Products were stored outside the drug label specifications.

What was recalled

Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10

Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
NDC code
55150-226-10
Origin
VA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0371-2024

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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