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TRUMATCH 420903Recalls & reported problems

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

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 10603295384786), 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. 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.

  • MalfunctionFeb 12, 2019Incorrect Measurement; Incorrect Measurement

    TRUMATCH CASES (B)(4) DID NOT PERFORM AS EXPECTED. IT WAS DISCUSSED THAT THE SURGEON DOES 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. HERE ARE CASE DETAILS: (B)(4).

    Patient problems: Not Applicable

    MAUDE report 8331228 ↗

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