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MatrixMANDIBLE 04.503.772Recalls & reported problems

Synthes GmbH · TI MATRIXMANDIBLE 7X23 ANGLE RECON PLATE LEFT 2.8MM THICK · Class 2 · Implant

All models of MatrixMANDIBLE (79)

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 10887587022994), received between Oct 8, 2018 and Oct 8, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • No Code Available1
  • Not Applicable1

Recent adverse event reports

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

  • InjuryOct 8, 2018Break; Break

    IT WAS REPORTED PATIENT WAS IMPLANTED WITH THE MATRIXMANDIBLE PLATE ON UNKNOWN DATE. ON UNKNOWN DATE IT WAS DETERMINED THE PLATE WAS BROKEN. PATIENT WAS RETURNED TO SURGERY WHERE THE PLATE WAS REMOVED. IT WAS FURTHER REPORTED PATIENT HAS UNDERGONE THREE (3) SURGERIES DUE TO BREAKAGE OF THIS AND SIMILAR PLATES.THIS REPORT IS FOR ONE (1) MATRIXMANDIBLE PLATE. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: No Code Available; Not Applicable

    MAUDE report 7943013 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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