Z-1015-2013 Class II Terminated
FDA device recall Z-1015-2013 was initiated by CareFusion Corporation on November 20, 2009 and is designated Class II. 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. The recall status is terminated (terminated March 28, 2013). Affected quantity: 2637.
Recall Details
- Product Type
- Devices
- Report Date
- April 3, 2013
- Initiation Date
- November 20, 2009
- Termination Date
- March 28, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2637
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.
Distribution Pattern
Worldwide Distribution - USA (Nationwide) including CANADA.
Code Information
All Pyxis Anesthesia System Model 2000