FDAFDA · Food and drugs·Recall number D-0638-2017
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
Published April 12, 2017 · Recall initiated: January 24, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc., A Pfizer Company
- Distributor
- U.S. Nationwide
- Lot
- Lot # 591053A, Exp 11/1/2017
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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