FDAFDA · Food and drugs·Recall number D-615-2013
5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48
Published July 3, 2013 · Recall initiated: May 4, 2012
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: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
- Lot
- Lot #: 11-161-JT, Exp 11/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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