---
title: "MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical s... — FDA record Z-1905-2025 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-1905-2025-mira-surgical-system-table-mounted-miniaturized-electromechanical-surgical-system-catalog-number-mir/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Soft... — FDA record Z-1905-2025

Reported completed

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 23, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3
- **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.
- **Classification**: Class II
- **Recalling firm**: VIRTUAL INCISION CORPORATION
- **Quantity**: 3 units
- **Agency-reported status**: Completed
- **Source record identifier**: Z-1905-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1905-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI (01)00850038042028; Lot Numbers: 1020040211, 1020040212, 1020040213 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Distribution to States: CA, FL, NE

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)

## Dates in the source

- **Report date**: Jun 11, 2025
- **Recall initiation date**: Apr 23, 2025
- **Center classification date**: Jun 4, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1905-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [VIRTUAL INCISION CORPORATION records](https://isitonrecall.com/brand/virtual-incision-corporation/)