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Medial Rotation Knee 156-612Recalls & reported problems

Matortho Ltd · Medial Rotation Knee Right Tibial Insert Size 1 10.5mm · Class 2 · Implant

Data updated Oct 18, 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 05055455503854), received between Jan 22, 2016 and Jan 22, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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

  • Improper or Incorrect Procedure or Method1
  • Off-Label Use1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryJan 22, 2016Off-Label Use; Improper or Incorrect Procedure or Method

    PATIENT UNDERWENT A LEFT TOTAL KNEE REPLACEMENT. FOLLOWING SURGERY, THE SCRUB NURSE IDENTIFIED THAT A RIGHT TIBIAL INSERT HAD BEEN USED, NOT A LEFT TIBIAL INSERT. PATIENT WAS INFORMED AND REVISED 1 DAY POST OP.

    Patient problems: No Code Available

    MAUDE report 5385130 ↗

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

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Sources and updates

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