Device recall
Z-0049-2025: KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090…
FDA device recall · Class I · Kinova Inc
Key facts
| Recall number (Z-number) | Z-0049-2025 |
|---|---|
| Recall event | 95065 |
| Product | KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body. |
| Product code | IQZ |
| Recalling firm | Kinova Inc |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3009538853 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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