Skip to content

My Knee Tibial Cutting Blocks 4.1084Recalls & reported problems

Medacta International SA · CT Left Lateral #4 · Class 2

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 07630030848711), received between Oct 31, 2017 and Oct 31, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Product Quality Problem” (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

  • Product Quality Problem1

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.

  • MalfunctionOct 31, 2017Product Quality Problem; Product Quality Problem

    THE MYKNEE TIBIAL CUTTING BLOCK WAS NOT USED DUE TO IMPINGEMENT WITH THE PATELLAR TENDON. THE SURGERY WAS COMPLETED SUCCESSFULLY USING THE CONVENTIONAL SYSTEM.

    Patient problems: No Code Available

    MAUDE report 6990399 ↗

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

How reports and recalls are matched · Editorial policy · Report an error on this page