US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 18, 2016 (10 years ago)

Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe…

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

Why it was recalled

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

What was recalled

Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15

Recalling firm
Cantrell Drug Company
NDC code
52533-064-15
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0202-2017

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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