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ADVANTIM® 18903310Recalls & reported problems

Microport Orthopedics Inc. · ADVANTIM® DURAMER® POST STAB TIBIAL INSERT LG/LG+ 10mm LSI · 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 M684189033101), received between Jan 19, 2021 and Jan 19, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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

  • Loosening of Implant Not Related to Bone-Ingrowth1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryJan 19, 2021Loosening of Implant Not Related to Bone-Ingrowth

    ALLEGEDLY, THE PATIENT WAS REVISED DUE TO CHRONIC KNEE PAIN, LOOSENING OF STEM AND COMPONENTS. (LEFT KNEE)

    Patient problems: Pain

    MAUDE report 11195307 ↗

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

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

Sources and updates

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