Pyxis Anesthesia System Model 2000 — Class II medical device recall Z-1015-2013
Terminated recall by CareFusion Corporation, reported 2013-04-03, distributed nationwide. The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessabilit
| Recall number | Z-1015-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion Corporation, San Diego, CA, United States |
| Recall initiated | 2009-11-20 |
| Classified | 2013-03-28 |
| Reported by FDA | 2013-04-03 |
| Terminated | 2013-03-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 2,637 |
| Model numbers | 2000 |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1015-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.