US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 5, 2022 (4 years ago)

Cyanocobalamin Injection, USP, 1,000 mcg per mL, For IM or SC Use Only, 1 mL Vial, Rx…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug: Out of Specification results for Assay

What was recalled

Cyanocobalamin Injection, USP, 1,000 mcg per mL, For IM or SC Use Only, 1 mL Vial, Rx Only, Manufactured in India, for Auromedics Pharma LLC, NDC 55150-364-01.

Recalling firm
Aurobindo Pharma USA Inc.
NDC code
55150-364-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0766-2022

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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