Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000 is an anesthesia ...
FDA Recall #Z-1015-2013 — Class II — November 20, 2009
Product Description
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.
Reason for Recall
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.
Recalling Firm
CareFusion Corporation — San Diego, CA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
2637
Distribution
Worldwide Distribution - USA (Nationwide) including CANADA.
Code Information
All Pyxis Anesthesia System Model 2000
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated