US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 6, 2014 (12 years ago)

Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial…

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

Why it was recalled

Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.

What was recalled

Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4332-01.

Recalling firm
Hospira Inc.
NDC code
0409-4332-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0387-2015

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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