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Advance KDHR1510Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® DOUBLE HIGH TIBIAL INSERT SIZE 1.5 RIGHT 10MM · Class 2 · Implant

All models of ADVANCE (147)

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 M684KDHR15101), received between Jan 27, 2020 and Jan 27, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Malposition of Device” (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

  • Malposition of Device1
  • Naturally Worn1

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.

  • InjuryJan 27, 2020Malposition of Device; Naturally Worn; Malposition of Device; Naturally Worn

    ALLEGEDLY, WHEN I TOOK IT OUT, THERE WAS A CLEAR DAMAGE TO THE INSIDE BACK. UPDATE 11-NOV-19: PRIMARY SURGERY DATE FOR THE PATIENT (B)(6) 2013.

    Patient problems: No Information

    MAUDE report 9633534 ↗

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

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Sources and updates

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