US Drug Recall Register
Class I · High risk Terminated Initiated Jan 24, 2017 (10 years ago)

Vancomycin Hydrochloride for Injection

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: A hair was found stuck to the stopper of inside a single vial. The hair came in contact with the reconstituted drug product.

What was recalled

Vancomycin Hydrochloride for Injection, USP, 10 grams, Pharmacy Bulk Package - Not For Direct Infusion, For Intravenous Use, packaged in 100 mL glass vial, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6510-01

Recalling firm
Hospira Inc., A Pfizer Company
NDC code
0409-6510-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0638-2017

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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