Device recall
Z-0139-2012: Picis Anesthesia Manager, PACU Manager,Critical Care Manager-8.2 Service Pack 4…
FDA device recall · Class II · Picis Inc.
Key facts
| Recall number (Z-number) | Z-0139-2012 |
|---|---|
| Recall event | 60006 |
| Product | Picis Anesthesia Manager, PACU Manager,Critical Care Manager-8.2 Service Pack 4 or higher (Software, transmission & storage, patient data) This product is a non-alarming software patient information system that compiles an electronic medical record utilizing commonly available hardware. A patient… |
| Product code | NSX |
| Recalling firm | Picis Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 23, 2012 |
| FEI number | 3005244943 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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