---
title: "Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF25... — FDA record Z-0290-2022 | Is It on Recall"
description: "During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube"
url: https://isitonrecall.com/recall/fda-device-z-0290-2022-endurant-stent-graft-system-ref-description-entf2525c70ee-stent-graft-entf2525c70ee-endurant-tube/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE — FDA record Z-0290-2022

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 15, 2021. 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**: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE
- **Reason**: During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube
- **Classification**: Class II
- **Recalling firm**: Medtronic Vascular, Inc.
- **Quantity**: 2 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0290-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0290-2022%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/Product Descripton: ENTF2525C70EE/STENT GRAFT ENTF2525C70EE ENDURANT TUBE GTIN Code: 00763000006129 Serial Numbers: V30624638 V30624639 |

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

## Distribution

Worldwide distribution - U.S. Nationwide distribution in the states of CA, FL, GA, MN, MO, NC, NJ, NM, NV, NY, PA, SC, TN, TX, VA, and WV. The countries of Austria, Belgium, Bulgaria, China, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Hungary, Ireland, Italy, Japan, Jordan, Lithuania, Luxembourg, Netherlands, Norway, Poland, Portugal, Qatar, South Africa, Spain, Sweden, Switzerland, and United Kingdom.

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**: Dec 1, 2021
- **Recall initiation date**: Oct 15, 2021
- **Center classification date**: Nov 24, 2021

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-0290-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Vascular, Inc. records](https://isitonrecall.com/brand/medtronic-vascular-inc/)
