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EVOLUTION EFXSNP6RRecalls & reported problems

Microport Orthopedics Inc. · Class 2 · Implant

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 M684EFXSNP6R1), received between Feb 17, 2021 and Feb 17, 2021 — classified as 1 injury.

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

  • Fracture1

Patient problems

  • Bone Fracture(s)1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryFeb 17, 2021Fracture

    ALLEGEDLY, PATIENT WAS REVISED ON (B)(6) 2018 DUE TO PROSTHETIC JOINT INFECTION WITH NONUNION OF PERIPROSTHETIC FEMUR FRACTURE. FEMORAL AND TIBIAL COMPONENTS, PATELLA REPLACED WITH NON-MPO IMPLANTS BY DIFFERENT SURGEON. (RIGHT KNEE)

    Patient problems: Bone Fracture(s); Unspecified Infection

    MAUDE report 11340273 ↗

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.