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MatrixMANDIBLE 04.503.733Recalls & reported problems

Synthes GmbH · TI MATRIXMANDIBLE 7X23H ANGLE RECON PL RIGHT 2.0MM 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 10887587022819), received between Nov 8, 2022 and Nov 8, 2022 — 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

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryNov 8, 2022Break; Break

    DEVICE REPORT FROM THE UNITED KINGDOM REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2022, THE RECON PLATE IN QUESTION BROKE IN-SITU A NUMBER OF MONTHS AFTER SURGERY. THE PLATE WAS ORIGINALLY PRE-BENT IN THE MAXFAC LAB AND STERILIZED BEFORE IMPLANTATION. THE PLATE NEEDS TO BE REMOVED AND REPLACED. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. THIS REPORT IS FOR A TI MATRIXMANDIBLE 7X23H ANGLE RECON PL RIGHT 2.0MM THICK. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: Failure of Implant

    MAUDE report 15751964 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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