Device recall
Z-2845-2026: Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge…
FDA device recall · Class II · Pride Mobility Products Corp.
Key facts
| Recall number (Z-number) | Z-2845-2026 |
|---|---|
| Recall event | 99286 |
| Product | Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller |
| Product code | ITI |
| Recalling firm | Pride Mobility Products Corp. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K042612 |
| FEI number | 3005068474 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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