FDAFDA · Food and drugs·Recall number D-0957-2017
0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015; Distributed in Canada by Baxter Corporation, Toronto, Ontario, Canada, Product Code: 2B1322, NDC 0338-0049-02.
Published July 19, 2017 · Recall initiated: July 6, 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
Lack of Assurance of Sterility: Customer complaints for leaking bags.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- Nationwide in USA
- Lot
- Lot: Y229153, Exp 09/30/18
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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