FDAFDA · Food and drugs·Recall number D-1591-2014
0.9% Sodium Chloride Injection USP, packaged in a) 50 mL VIAFLEX Container bags, NDC 0338-0049-41, Product Code 2B1306; and b) 100 mL VIAFLEX Container bags, NDC 0338-0049-18, Product Code 2B1302, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA.
Published September 24, 2014 · Recall initiated: July 11, 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
Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corp.
- Distributor
- Nationwide, Puerto Rico, Singapore, and Hong Kong
- Lot
- Lot #: a) P309187, Exp 10/14; b) P298190, Exp 08/14
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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