Device recall
Z-1102-2023: WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton…
FDA device recall · Class II · Wishbone Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1102-2023 |
|---|---|
| Recall event | 91526 |
| Product | WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS 10-702-095115-0 Short 10-702-115150-0 Medium 10-702-140200 Long 10-702-190300-0 |
| Product code | KTT |
| Recalling firm | Wishbone Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K193368 |
| FEI number | 3013680140 |
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