Device recall
Z-2332-2012: Sunquest Laboratory Sunquest Laboratory is intended for use by professionals…
FDA device recall · Class II · Sunquest Information Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2332-2012 |
|---|---|
| Recall event | 62768 |
| Product | Sunquest Laboratory Sunquest Laboratory is intended for use by professionals working in a clinical laboratory. Sunquest Laboratory is intended for use only by professionals who have received extensive training in the use of the software. Sunquest Laboratory is controlled via userdefined security… |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 2, 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