# FDA recall Z-0699-2025

> **MicroPort Orthopedics Inc.** · Class II · device recall initiated 2024-10-29.

## 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 for recall

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.

## Distribution

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

## Key facts

- **Recall number:** Z-0699-2025
- **Recalling firm:** MicroPort Orthopedics Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-29
- **Report date:** 2024-12-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0699-2025

## Citation

> AI Analytics. FDA recall Z-0699-2025. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0699-2025. Source: US FDA. Licensed CC0.

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