---
title: "KliniTray. KlinioTray. Tissue resection margin examination board/small. Model... — FDA record Z-1768-2025 | Is It on Recall"
description: "Potential for microbial contamination."
url: https://isitonrecall.com/recall/fda-device-z-1768-2025-klinitray-kliniotray-tissue-resection-margin-examination-board-small-model-number-2001105-f-the-medi/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device Kl... — FDA record Z-1768-2025

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 Apr 4, 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**: KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and positioning of tissue to be removed in the patient's body, enabling improved surgical precision and patient safety.
- **Reason**: Potential for microbial contamination.
- **Classification**: Class II
- **Recalling firm**: Klinika Mdical Gmb
- **Quantity**: 620 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1768-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1768-2025%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 | Model Number: 2001105-F. UDI-DI: 4053185001177. Lot Number: 25.019.01 |

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

## Distribution

US Nationwide distribution in the state of Massachusetts.

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 21, 2025
- **Recall initiation date**: Apr 4, 2025
- **Center classification date**: May 15, 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-1768-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Klinika Mdical Gmb records](https://isitonrecall.com/brand/klinika-mdical-gmb/)
