---
title: "FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft — FDA record Z-2004-2024 | Is It on Recall"
description: "Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces."
url: https://isitonrecall.com/recall/fda-device-z-2004-2024-flixene-6x40-1gds-gw-single-ended-slider-gds-vascular-graft/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft — FDA record Z-2004-2024

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 May 3, 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**: FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
- **Reason**: Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- **Classification**: Class II
- **Recalling firm**: Atrium Medical Corporation
- **Quantity**: 53,308 units (US: 11, 236; OUS: 42,072)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2004-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2004-2024%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 Code: 25061; UDI-DI: 00650862250619. |

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

## Distribution

Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB, GR, HK, ID, IE, IL, IQ, IT, JO, JP, KR, KW, LT, LU, LV, ME, MN, MU, MX, MY, NI, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, PY, RO, RU, SA, SE, SG, SI, SV, TH, TN, TR, TW, UA, VN, XK, YE, ZA.

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**: Jun 12, 2024
- **Recall initiation date**: May 3, 2024
- **Center classification date**: Jun 4, 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-2004-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Atrium Medical Corporation records](https://isitonrecall.com/brand/atrium-medical-corporation/)
