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ADVANCE® KIDH217LRecalls & reported problems

Microport Orthopedics Inc. · ADVANCE® DOUBLE HIGH TIBIAL INSERT SIZE 2 LEFT 17MM · 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 M684KIDH217L1), received between Oct 8, 2020 and Oct 8, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1
  • Loss of Osseointegration1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryOct 8, 2020Loss of Osseointegration; Detachment of Device or Device Component; Loss of Osseointegration; Detachment of Device or Device Component

    ALLEGEDLY, TIBIAL INSERT WAS FOUND TO BE LOOSE FROM THE TIBIAL BASE. PATIENT HAD HER FIRST REVISION ON (B)(6) 2020 , IT WAS CAPTURED UNDER INCIDENT NUMBER : (B)(4).

    Patient problems: No Information

    MAUDE report 10652409 ↗

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.