Device recall
Z-0423-03: Misys Laboratory versions 5.23 and 5.3
FDA device recall · Class II · Sunquest Information Systems
Key facts
| Recall number (Z-number) | Z-0423-03 |
|---|---|
| Recall event | 25212 |
| Product | Misys Laboratory versions 5.23 and 5.3 |
| Recalling firm | Sunquest Information Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2003 |
| FEI number | 1000306472 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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