FDAFDA · Food and drugs·Recall number D-1240-2015
0.9% Sodium Chloride Injection USP, 50 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira, Inc., Ausitn, TX 78728, NDC 00409-7101-68
Published July 22, 2015 · Recall initiated: July 2, 2015
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
Lack of assurance of sterility: Potential channel leaks near the threaded vial port.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- United States
- Lot
- Lot #: 49-084-JT; 49-119-JT
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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