Device recall
Z-1727-2025: iGo2 DC Car Adapter to be used with iGo2 Portable Oxygen Concentrator Systems…
FDA device recall · Class I · Medical Depot Inc.
Key facts
| Recall number (Z-number) | Z-1727-2025 |
|---|---|
| Recall event | 96700 |
| Product | iGo2 DC Car Adapter to be used with iGo2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle. |
| Product code | CAW |
| Recalling firm | Medical Depot Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K071397 |
| FEI number | 3002997602 |
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