MatrixMANDIBLE 03.503.910Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887587013251), received between Jul 14, 2022 and Jul 14, 2022 — 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

Recent adverse event reports

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

• MalfunctionJul 14, 2022Break; Break

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN COLUMBIA AS FOLLOWS: DURING THE SURGICAL PROCEDURE, THE SIZE OF THE PREMOLDED PLATES WERE BEING MEASURED, AS THEY ARE SO FRAGILE THEY SPLIT, BUT THERE WAS NO INCONVENIENCE BECAUSE THERE WERE OTHERS USED. SURGERY ENDED WITHOUT COMPLICATION. THIS REPORT IS FOR ONE (1) MATRIXMANDIBLE BINDNG TEMPLATE F/PREFORMED RECON PL/SMALL THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15015113 ↗