---
title: "Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Se... — FDA record Z-0363-2025 | Is It on Recall"
description: "Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S."
url: https://isitonrecall.com/recall/fda-device-z-0363-2025-irrigation-tubing-for-karl-storz-endomat-select-up210-ref-031523-10-tubing-set-irrigation-pc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC — FDA record Z-0363-2025

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 Oct 21, 2024. 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**: Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC
- **Reason**: Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S.
- **Classification**: Class II
- **Recalling firm**: Karl Storz Endoscopy
- **Quantity**: 40 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0363-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0363-2025%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 | Product/Material Number: 031523-10 UDI-DI code: 04048438006306 Lot Number: 240222 |

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

## Distribution

U.S. Nationwide distribution in the states of CO, CT, DC, MD, MI, MN, NC, NY, OH, OK, TN, TX, WA.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Nov 20, 2024
- **Recall initiation date**: Oct 21, 2024
- **Center classification date**: Nov 12, 2024

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-0363-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Karl Storz Endoscopy records](https://isitonrecall.com/brand/karl-storz-endoscopy/)