Device recall
Z-0319-03: Misys Laboratory version 5.2 with Results Interface 14
FDA device recall · Class II · Sunquest Information Systems
Key facts
| Recall number (Z-number) | Z-0319-03 |
|---|---|
| Recall event | 25074 |
| Product | Misys Laboratory version 5.2 with Results Interface 14 |
| Product code | JQP |
| Recalling firm | Sunquest Information Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 1, 2004 |
| 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