FDAFDA · Food and drugs·Recall number Z-1015-2013
Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000 is an anesthesia medication dispensing device that provides medications and inventory management for the anesthesiologist at the point of care within the operating room.
Published April 3, 2013 · Recall initiated: November 20, 2009
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
The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessability of drawers caused by system down time or lock-up.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CareFusion Corporation
- Distributor
- Worldwide Distribution - USA (Nationwide) including CANADA.
- Lot
- All Pyxis Anesthesia System Model 2000
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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