TRUMATCH 420901Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295384762), received between Nov 16, 2017 and Jan 24, 2019 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Fitting 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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 24, 2019Fitting Problem; Fitting Problem

  IT WAS REPORTED THAT THE TIBIA BLOCK DID NOT FIT FOR CASE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8273753 ↗
• MalfunctionDec 27, 2018Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  IT WAS REPORTED THAT THE SIZING WAS OFF.

  Patient problems: No Consequences Or Impact To Patient; Not Applicable

  MAUDE report 8200045 ↗
• MalfunctionNov 16, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT TRUMATCH FEMORAL AND TIBIAL BLOCKS DID NOT FIT WELL AT ALL. BOTH CUTS HAD TO BE ADJUSTED.

  Patient problems: No Information

  MAUDE report 7037104 ↗