Device recall
Z-1015-2013: Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000 is an…
FDA device recall · Class II · CareFusion Corporation
Key facts
| Recall number (Z-number) | Z-1015-2013 |
|---|---|
| Recall event | 53991 |
| 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. |
| Product code | BRY |
| Recalling firm | CareFusion Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2013 |
| FEI number | 2016493 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database