Device recall
Z-0653-05: Nonin Xpod Oximeter model numbers 3011 and 3012, distributed for use with the…
FDA device recall · Class II · Compumedics Usa, Ltd
Key facts
| Recall number (Z-number) | Z-0653-05 |
|---|---|
| Recall event | 31197 |
| Product | Nonin Xpod Oximeter model numbers 3011 and 3012, distributed for use with the Compumedics E-Series Digital Amplifier. |
| Product code | GWQ |
| Recalling firm | Compumedics Usa, Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 7, 2007 |
| FEI number | 3002716534 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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