FDAFDA · Food and drugs·Recall number D-0123-2018
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
Published December 27, 2017 · Recall initiated: August 30, 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: glass particulate found in vial
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Brand
- VANCOMYCIN HYDROCHLORIDE
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide USA and Puerto Rico
- Lot
- Lot: 632153A; Exp. 03/18
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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