FDAFDA · Food and drugs·Recall number D-0334-2015
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
Published January 14, 2015 · Recall initiated: December 22, 2014
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: The product has the potential for solution to leak at the administrative port.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 42-306-C6
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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