Class II — VIRTUAL INCISION CORPORATION
| Recalling firm | Virtual Incision Corporation |
|---|---|
| Registered facility | VIRTUAL INCISION CORPORATION (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential to exhibit interrupted motion on the display screen, caused by a software latency between the movement of the hand controllers and the movement of the Surgical Minibot arms. |
| Product | MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3 |
| Quantity | 3 units |
| Distribution | US Distribution to States: CA, FL, NE |
| Initiated | 2025-04-23 |
| Classified | 2025-06-04 |
| Recall number | Z-1905-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — VIRTUAL INCISION CORPORATION (Z-1905-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96831/
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