FDAFDA · Food and drugs·Recall number Z-1830-2020
Prismaflex System, Prismaflex Control Unit
Published May 6, 2020 · Recall initiated: February 6, 2020
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
Baxter is communicating safety information from the Prismaflex Operator's Manual regarding the proper use of connectors with the Prismaflex system.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- Distribution in US, Puerto Rico
- Lot
- Product Code: 114870; GTIN 07332414115395
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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