Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The Recalled by CareFusion Corporation Due to The recall was initiated because Carefusion has confirmed...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact CareFusion Corporation directly.
Affected Products
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.
Quantity: 2637
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CareFusion Corporation
CareFusion Corporation has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report