---
title: "ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of ELEOS... — FDA record Z-1857-2025 | Is It on Recall"
description: "Potential challenge with intraoperative assembly of the external taper of a single midsection with the internal taper of a mating proximal femur."
url: https://isitonrecall.com/recall/fda-device-z-1857-2025-eleos-male-female-midsection-40mm-part-number-25001040e-component-of-eleos-limb-salvage-system/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of ELEOS Limb Salvage System — FDA record Z-1857-2025

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 Sep 22, 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**: ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of ELEOS Limb Salvage System
- **Reason**: Potential challenge with intraoperative assembly of the external taper of a single midsection with the internal taper of a mating proximal femur.
- **Classification**: Class II
- **Recalling firm**: Onkos Surgical, Inc.
- **Quantity**: 24 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1857-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1857-2025%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 | Part Number: 25001040E. UDI-DI B27825001040E0. Lot Numbers: 1989873, 1989874 |

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

## Distribution

US Nationwide distribution in the states of AZ, CA, FL, FL, MD, MO, NC, TN.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Arizona](https://isitonrecall.com/state/arizona/)
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- [Hawaii](https://isitonrecall.com/state/hawaii/)
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- [Idaho](https://isitonrecall.com/state/idaho/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 4, 2025
- **Recall initiation date**: Sep 22, 2024
- **Center classification date**: May 28, 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-1857-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Onkos Surgical, Inc. records](https://isitonrecall.com/brand/onkos-surgical-inc/)