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Advance KTTIHA11Recalls & reported problems

Microport Orthopedics Inc. · ADVANCE® HA COATED TITANIUM TIBIAL BASE SIZE 1+ · 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 M684KTTIHA111), received between May 30, 2022 and May 30, 2022 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1
  • Fracture1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryMay 30, 2022Fracture; Appropriate Device Problem Term/Code Not Available

    ALLEGEDLY, PATIENT WAS REVISED DUE TO PERI-PROSTHETIC FRACTURE. SRNJR NUMBER: (B)(4). SIDE:R. FRASA: P2 - MILD DISEASE NOT INCAPACITATING.

    Patient problems: Bone Fracture(s)

    MAUDE report 14545125 ↗

Other Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer devices

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Sources and updates

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