Device recall
Z-1780-2012: NIDEK Medical NUVO LITE MODEL 925 OCSI, 230V - 50Hz - 300W. Oxygen Concentrator.
FDA device recall · Class I · Nidek Medical Products Inc
Key facts
| Recall number (Z-number) | Z-1780-2012 |
|---|---|
| Recall event | 61843 |
| Product | NIDEK Medical NUVO LITE MODEL 925 OCSI, 230V - 50Hz - 300W. Oxygen Concentrator. |
| Product code | CAW |
| Recalling firm | Nidek Medical Products Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 21, 2017 |
| 510(k) numbers | K032509 |
| FEI number | 1039215 |
At a glance
- 1–9 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