US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 25, 2019 (7 years ago)

Vancomycin Hydrochloride for Injection, USP, 1 g* per vial, packaged in 10-count vials…

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

Why it was recalled

Discoloration: Product complaints of discoloration after reconstitution of vials.

What was recalled

Vancomycin Hydrochloride for Injection, USP, 1 g* per vial, packaged in 10-count vials per carton, Rx only, Mft. in India for: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-204-20.

Recalling firm
AuroMedics Pharma LLC
NDC code
55150-204-20
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0574-2020

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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