# FDA recall Z-2244-2024

> **MicroPort Orthopedics Inc.** · Class II · device recall initiated 2024-05-03.

## Product

EVOLUTION¿ MP Femoral CS/CR Non-Porous    Non-porous MicroPort total knee replacement implants are for cemented use only.

## Reason for recall

One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3 Evolution MP Non-Porous Femoral Left in the packaging.

## Distribution

International distribution in the country of China. There is no field inventory in the United States for either lot.

## Key facts

- **Recall number:** Z-2244-2024
- **Recalling firm:** MicroPort Orthopedics Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-03
- **Report date:** 2024-07-10

- **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-2244-2024

## Citation

> AI Analytics. FDA recall Z-2244-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2244-2024. Source: US FDA. Licensed CC0.

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