Skip to content

TRUMATCH 420902Recalls & reported problems

Depuy Orthopaedics, Inc. · TruMatch FEMORAL PIN GUIDE FOR USE WITH: LEFT · Class 2

All models of TRUMATCH (5)

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 10603295384779), received between Feb 12, 2019 and Feb 12, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect Measurement” (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

  • Incorrect Measurement1

Patient problems

  • Not Applicable1

Recent adverse event reports

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

  • MalfunctionFeb 12, 2019Incorrect Measurement; Incorrect Measurement

    TRUMATCH CASES (B)(4) DID NOT PERFORM AS EXPECTED. IT WAS DISCUSSED THAT THE SURGEON DID NOT CLEAR THE ANTERIOR SOFT TISSUE OF THE FEMUR. PER OUR SURGICAL TECHNIQUE, IT IS RECOMMENDED TO CLEAR EXTRANEOUS SOFT TISSUE FROM THE ANTERIOR ASPECT OF THE FEMUR.

    Patient problems: Not Applicable

    MAUDE report 8331231 ↗

Other Knee arthroplasty implantation system devices

All Knee arthroplasty implantation system devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page