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TRUMATCH 420918Recalls & reported problems

Depuy (Ireland) · TRUMATCH PERSONALIZED SOLUTIONS RESECTION GUIDE FEMUR - CT KNEE FOR USE WITH: RIGHT · Class 3

All models of TRUMATCH (10)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295384885), received between Jun 17, 2022 and Aug 8, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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 16, 2026.

Most reported problems

Device problems

  • Break2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 8, 2022Break; Break

    IT WAS REPORTED THAT THE METAL SAW CAPTURE IN TRUMATCH CAME OUT OF GUIDE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15182953 ↗
  • MalfunctionJun 17, 2022Break; Break

    IT WAS REPORTED THAT THE METAL SAW CAPTURE VIBRATED OUT OF THE TRUMATCH FEMORAL CUTTING GUIDE. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14737385 ↗

Other Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing devices

All Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing devices →

Sources and updates

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