---
title: "EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5... — FDA record Z-0699-2025 | Is It on Recall"
description: "Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packagin"
url: https://isitonrecall.com/recall/fda-device-z-0699-2025-evolution-mp-femoral-component-cs-cr-porous-size-5-right-primary-ref-efsrp5pr-evolution-mp-femoral-c/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR... — FDA record Z-0699-2025

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 Oct 29, 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**: EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis component
- **Reason**: Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
- **Classification**: Class II
- **Recalling firm**: MicroPort Orthopedics Inc.
- **Quantity**: 32
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0699-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0699-2025%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 | REF/UDI-DI/Lot/Expiration: EFSRP5PR/M684EFSRP5PR1/2007116/2032-05-06. EFSRN6PL/M684EFSRN6PL1/MP2002559/2032-05-06. |

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

## Distribution

OUS: CN, GR, ES, ZA, FR, JP, IT

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

## Dates in the source

- **Report date**: Dec 25, 2024
- **Recall initiation date**: Oct 29, 2024
- **Center classification date**: Dec 18, 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-0699-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MicroPort Orthopedics Inc. records](https://isitonrecall.com/brand/microport-orthopedics-inc/)