Device recall
Z-2272-2012: Sunquest Laboratory LabAccess Results Workstation (LARS)
FDA device recall · Class II · Sunquest Information Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2272-2012 |
|---|---|
| Recall event | 62714 |
| Product | Sunquest Laboratory LabAccess Results Workstation (LARS) |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 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