Device recall
Z-0410-2026: Brand Name: Medistim MiraQ System Product Name: Medistim MiraQ System…
FDA device recall · Class II · Medistim Asa
Key facts
| Recall number (Z-number) | Z-0410-2026 |
|---|---|
| Recall event | 97707 |
| Product | Brand Name: Medistim MiraQ System Product Name: Medistim MiraQ System Model/Catalog Number: MQC04001, MQC14001, MQU14011, MQV12011 Software Version: Not applicable Product Description: Ultrasound device for intraoperative use Component: No |
| Product code | DPW |
| Recalling firm | Medistim Asa |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K102595 |
| 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