Device recall
Z-1827-2026: WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is…
FDA device recall · Class I · WHILL, INC.
Key facts
| Recall number (Z-number) | Z-1827-2026 |
|---|---|
| Recall event | 98320 |
| Product | WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair. |
| Product code | ITI |
| Recalling firm | WHILL, INC. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K221438 |
| FEI number | 3021071770 |
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