Recall Z-1015-2013— CareFusion Corporation
Class II · Terminated
Class II FDA medical device recall by CareFusion Corporation, initiated 2009-11-20, terminated 2013-03-28. FDA's recall record names no specific 510(k) clearance for this event. Product: 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: 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
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2009-11-20
- Terminated
- 2013-03-28
- Firm location
- San Diego, CA, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.