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Evolution EIS6S17LRecalls & reported problems

Microport Orthopedics Inc. · EVOLUTION® MP™ CS INSERT SIZE 6 STANDARD 17MM LEFT · Class 2 · Implant

Data updated Oct 13, 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 M684EIS6S17L1), received between Jul 10, 2023 and Jul 10, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJul 10, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, PATIENT UNDERWENT L TKR ON (B)(6) 2020. REVISED ON (B)(6) 2023 DUE TO INFECTION. 17MM INSERT REPLACED WITH ONE OF THE SAME SIZE.

    Patient problems: Unspecified Infection

    MAUDE report 17293253 ↗

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

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Sources and updates

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