---
title: "Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in ... — FDA record Z-1468-2023 | Is It on Recall"
description: "A packaging defect may compromise the sterile barrier."
url: https://isitonrecall.com/recall/fda-device-z-1468-2023-mani-trocar-kit-model-mtk23s-and-model-mtk25s-there-are-3-kits-contained-in-one-box-and-sterile-1-ki/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3... — FDA record Z-1468-2023

Reported terminated

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 Feb 20, 2023. 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**: Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar with the valved cannula and 1 pc. infusion cannula.
- **Reason**: A packaging defect may compromise the sterile barrier.
- **Classification**: Class II
- **Recalling firm**: Mani, Inc. - Kiyohara Facility
- **Quantity**: 45 kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1468-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1468-2023%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: 14546951403956 (Model MTK25S) Mani Trocar Kit: 1) Model MTK23S, Lot V210028903 (exp. 2024-03) 2) Model MTK25S, Lot V210009900 (exp. 2023-03) 3) Model MTK25S, Lot V210006701 (exp. 2023-04) 4) Model MTK25S, Lot V210009101 (exp. 2023-11) 5) Model MTK25S, Lot V220016001 (exp. 2024-11-08) |

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

## Distribution

Distribution in US - 1 consignee in Missouri

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

- [Missouri](https://isitonrecall.com/state/missouri/)

## Dates in the source

- **Report date**: May 3, 2023
- **Recall initiation date**: Feb 20, 2023
- **Center classification date**: Apr 26, 2023
- **Termination date**: May 19, 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-1468-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mani, Inc. - Kiyohara Facility records](https://isitonrecall.com/brand/mani-inc-kiyohara-facility/)