---
title: "Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for uro... — FDA record Z-1443-2026 | Is It on Recall"
description: "Complaints of the ceramic tip of the resection sheath breaking have been received."
url: https://isitonrecall.com/recall/fda-device-z-1443-2026-olympus-resection-sheath-26-fr-model-no-a22042a-resection-sheath-for-urologic-applications/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications. — FDA record Z-1443-2026

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 Nov 11, 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**: Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.
- **Reason**: Complaints of the ceramic tip of the resection sheath breaking have been received.
- **Classification**: Class II
- **Recalling firm**: Olympus Corporation of the Americas
- **Quantity**: 1,676 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1443-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1443-2026%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 | Model No. A22042A; UDI: 04042761020985; All Lots. |

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

## Distribution

US Nationwide Distribution.

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**: Mar 4, 2026
- **Recall initiation date**: Nov 11, 2025
- **Center classification date**: Feb 20, 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-1443-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Olympus Corporation of the Americas records](https://isitonrecall.com/brand/olympus-corporation-of-the-americas/)