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Evolution EIS3S10RRecalls & reported problems

Microport Orthopedics Inc. · EVOLUTION® MP™ CS INSERT SIZE 3 STANDARD 10MM 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 M684EIS3S10R1), received between Jun 19, 2023 and Jun 19, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (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

  • Unstable1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryJun 19, 2023Unstable; Unstable

    ALLEGEDLY, PATIENT UNDERWENT R TKR ON (B)(6) 2021. REVISED ON (B)(6) 2023 AS KNEE WAS UNSTABLE AND FELT LOOSE. 10MM TIBIAL INSERT REPLACED WITH A 14MM ONE. AUSTRALIA-C23-244.

    Patient problems: Insufficient Information

    MAUDE report 17153296 ↗

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Sources and updates

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