Device recall
Z-0719-2018: MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that…
FDA device recall · Class II · Medistim Asa
Key facts
| Recall number (Z-number) | Z-0719-2018 |
|---|---|
| Recall event | 78973 |
| Product | MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions. |
| Product code | DPW |
| Recalling firm | Medistim Asa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2024 |
| 510(k) numbers | K040228 |
| FEI number | 3010790133 |
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