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Evolution EFSRN2PRRecalls & reported problems

Microport Orthopedics Inc. · EVOLUTION®MP FEM CS/CR NON-POR SIZE 2 PRIMARY RIGHT · Class 2 · Implant

All models of Evolution (125)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684EFSRN2PR1), received between May 17, 2021 and May 17, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 17, 2021Break; Break

    ALLEGEDLY, PATIENT CONSULTED THE PHYSICIAN DUE TO PAIN. AFTER X-RAY PHOTOGRAPH, IT'S FOUND THE PROSTHESIS GOT BROKEN. THE BACK PART OF THE FEMORAL COMPONENT IS CRACKED. NO REVISION SURGERY HAS BEEN CONDUCTED YET.

    Patient problems: Pain

    MAUDE report 11832415 ↗

Other Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer devices

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Sources and updates

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