Device recall
Z-2243-2012: Sunquest Encompass The reporting site is using the Encompass software in an…
FDA device recall · Class III · Sunquest Information Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2243-2012 |
|---|---|
| Recall event | 62751 |
| Product | Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting. |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 22, 2012 |
| FEI number | 1000306472 |
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