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Medial Rotation Knee 156-023Recalls & reported problems

Matortho Ltd · Medial Rotation Knee Femoral Component Pegged Right F3 · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055455503465), received between Jan 22, 2016 and Jan 22, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Packaging Compromised” (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 18, 2026.

Most reported problems

Device problems

  • Device Packaging Compromised1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionJan 22, 2016Device Packaging Compromised

    DAMAGE NOTICED TO OUTER STERILE BARRIER PACKAGING. IDENTIFIED PRIOR TO USE AND ALTERNATIVE DEVICE AVAILABLE FOR IMMEDIATE USE.

    Patient problems: No Patient Involvement

    MAUDE report 5385133 ↗

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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