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TRUMATCH 420580Recalls & reported problems

Depuy Orthopaedics, Inc. · TRUMATCH PERSONALIZED SOLUTIONS PIN GUIDE FEMUR - CT KNEE FOR USE WITH: LEFT · Class 3

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 10603295430810), received between Jun 13, 2019 and Jun 13, 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. How this data works · Data updated Oct 13, 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.

  • MalfunctionJun 13, 2019Incorrect Measurement; Incorrect Measurement

    THERE WAS AN APPROXIMATELY 5 MINUTES DELAY.

    Patient problems: Not Applicable

    MAUDE report 8695780 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.