Device recall
Z-0874-03: OmniDiagnost System
FDA device recall · Class II · Philips Medical Systems Sales & Service Region No. America
Key facts
| Recall number (Z-number) | Z-0874-03 |
|---|---|
| Recall event | 26837 |
| Product | OmniDiagnost System |
| Recalling firm | Philips Medical Systems Sales & Service Region No. America |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2005 |
| 510(k) numbers | K982993 |
| FEI number | 1000524572 |
At a glance
- 1–9 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