US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 7, 2014 (12 years ago)

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml…

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

Why it was recalled

Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.

What was recalled

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.

Recalling firm
Hospira Inc.
NDC code
0409-6533-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0254-2015

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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