FDAFDA · Food and drugs·Recall number D-1177-2017
Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24
Published October 4, 2017 · Recall initiated: September 1, 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
Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide in the USA
- Lot
- Lot: 63-075-DK Exp. FEB 2019
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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