FDA Drug Recalls

Recalls / Active ingredient / Vancomycin Hydrochloride

Vancomycin Hydrochloride

7 FDA drug recalls involving the active ingredient “Vancomycin Hydrochloride” — 3 Class I.

DateClassProductFirm
2024-03-21Class IVancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL, packaged as (a) 80 mL bottle, NDC 69238-2261Amneal Pharmaceuticals of New York, LLC
2022-12-22Class IVancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials pPfizer Inc.
2019-11-25Class IIVancomycin Hydrochloride for Injection, USP, 1 g* per vial, packaged in 10-count vials per carton, Rx only, MfAuroMedics Pharma LLC
2017-08-30Class IVancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL Pfizer Inc.
2014-11-07Class IIISterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count Hospira Inc.
2014-10-06Class IIVancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per Hospira Inc.
2014-10-06Class IIVancomycin Hydrochloride for Injection, USP, 1 g Sterile Powder per Fliptop Vial, packaged in 10 Units per carHospira Inc.