---
title: "Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.; — FDA record Z-2068-2026 | Is It on Recall"
description: "If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be los"
url: https://isitonrecall.com/recall/fda-device-z-2068-2026-mint-lesion-software-versions-3-4-0-up-to-3-9-5/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.; — FDA record Z-2068-2026

Reported ongoing

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 Jan 7, 2026. 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**: Mint Lesion; Software Versions: 3.4.0 up to 3.9.5.;
- **Reason**: If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.
- **Classification**: Class II
- **Recalling firm**: Mint Medical GmbH
- **Quantity**: 101 systems
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2068-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2068-2026%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 | Software Versions: 3.4.0 up to 3.9.5. UDI-DI: 04260495880341, 04260495880358, 04260495880365, 04260495880372, 04260495880389, 04260495880396. |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of Germany, Switzerland, Austria, Belgium, Italy, France, Romania, Netherlands, United Kingdom, Spain, Czech Republic, Ireland, Poland;

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

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## Dates in the source

- **Report date**: May 13, 2026
- **Recall initiation date**: Jan 7, 2026
- **Center classification date**: May 6, 2026

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-2068-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mint Medical GmbH records](https://isitonrecall.com/brand/mint-medical-gmbh/)
