Device recall
Z-0143-04: Datex-Ohmeda Cardiocap/5 Patient Monitors
FDA device recall · Class III · Datex-Ohmeda Inc
Key facts
| Recall number (Z-number) | Z-0143-04 |
|---|---|
| Recall event | 27599 |
| Product | Datex-Ohmeda Cardiocap/5 Patient Monitors |
| Product code | MHX |
| Recalling firm | Datex-Ohmeda Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 15, 2005 |
| 510(k) numbers | K012837 |
| FEI number | 2183066 |
At a glance
- 1–9 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