Device recall
Z-0806-03: Misys Commercial Laboratory, Laboratory Information System, version 3.4.1
FDA device recall · Class III · Misys Healthcare Systems
Key facts
| Recall number (Z-number) | Z-0806-03 |
|---|---|
| Recall event | 26042 |
| Product | Misys Commercial Laboratory, Laboratory Information System, version 3.4.1 |
| Recalling firm | Misys Healthcare Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 14, 2004 |
| 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