Device recall
Z-2539-2025: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in…
FDA device recall · Class I · Max Mobility LLC
Key facts
| Recall number (Z-number) | Z-2539-2025 |
|---|---|
| Recall event | 97356 |
| Product | Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component. |
| Product code | ITI |
| Recalling firm | Max Mobility LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K151199 |
| FEI number | 3008370857 |
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