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MatrixMANDIBLE 03.503.181Recalls & reported problems

Synthes GmbH · MATRIXMANDIBLE BENDNG TEMPLATE F/2.5/2.8MM ANGLE RECON PLATE · Class 1

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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887587012445), received between Dec 2, 2021 and Dec 2, 2021 — classified as 1 malfunction.

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 Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionDec 2, 2021Break; Break

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING A ROUTINE INCOMING INSPECTION OF A LOANER SET AT FIELD STOCKING LOCATION(FSL) UPS (B)(6), IT WAS OBSERVED THAT MATRIXMAND BND TMPL 2.5/2.8 ANG RECON PL WAS BROKEN. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS COMPLAINT INVOLVES ONE(1) DEVICE. THIS REPORT IS FOR (1) MATRIXMANDIBLE BENDING TEMPLATE F/2.5/2.8MM ANGLE RECON PLATES THIS IS REPORT 1 OF 1 FOR COMPLAINT: (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12919575 ↗

Other TEMPLATE devices

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Sources and updates

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