---
title: "ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection... — FDA record Z-0147-2026 | Is It on Recall"
description: "The devices were shipped unsterilized."
url: https://isitonrecall.com/recall/fda-device-z-0147-2026-echelon-linear-cutters-reload-80-mm-blue-intended-for-transection-resection-and-or-creation-of-anast/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Produc... — FDA record Z-0147-2026

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 Sep 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**: ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80
- **Reason**: The devices were shipped unsterilized.
- **Classification**: Class II
- **Recalling firm**: Ethicon Endo-Surgery Inc
- **Quantity**: 3 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0147-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0147-2026%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 | UDI-DI: 10705036030881; Lot Number: 904C12 |

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

## Distribution

International distribution to the countries of United Arab Emirates.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 22, 2025
- **Recall initiation date**: Sep 11, 2025
- **Center classification date**: Oct 14, 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-0147-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Ethicon Endo-Surgery Inc records](https://isitonrecall.com/brand/ethicon-endo-surgery-inc/)