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TRUMATCH ATTUNE 420946Recalls & reported problems

Depuy Orthopaedics, Inc. · TRUMATCH Resection GUIDE Set for Attune FOR USE WITH: RIGHT · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295431800), received between Jan 4, 2018 and Aug 29, 2023 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Defective Device1
  • Fracture1
  • Patient-Device Incompatibility1

Patient problems

  • No Consequences Or Impact To Patient3
  • Unspecified Tissue Injury1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 29, 2023Patient-Device Incompatibility; Patient-Device Incompatibility

    IT WAS REPORTED THAT THERE WERE A RECENT NUMBER OF CASES THAT HAVE HAD INCORRECT VALGUS ANGLES AND ALSO THAT THE TIBIAL RESECTION GUIDES WERE NOT CUTTING TO PERPENDICULAR OF THE MECHANICAL AXIS.

    Patient problems: Unspecified Tissue Injury

    MAUDE report 17641532 ↗
  • MalfunctionMar 25, 2019Break; Break

    TRU MATCH TIBIAL CUT BLOCK BROKE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8450446 ↗
  • MalfunctionSep 12, 2018Defective Device; Defective Device

    IT WAS REPORTED THAT A CASE THAT WAS DESIGNED WITH DIFFERENT TIBIA RESECTION FROM SURGEONS SURGICAL PREFERENCES, DUE TO A SYSTEM GLITCH. THE PROPOSAL WAS NOT DESIGNED TO SURGEON PREFERENCES BUT WAS APPROVED BY THE SURGEON. SURGERY HAS NOT TAKEN PLACE BUT IS SCHEDULED FOR MONDAY (B)(6) 2018. THE SALES REP AND SURGEON ARE AWARE OF THE RESECTION CHANGE AND WILL ADJUST RESECTION CUTS INTRAOPERATIVELY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7869945 ↗
  • MalfunctionJan 4, 2018Fracture; Fracture

    IT WAS REPORTED THAT THE FEMORAL RESECTION BLOCK BROKE DURING RESECTION. THE SAW BLADE WILL BE INCLUDED WITH BLOCKS AND BE RETURNED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7163624 ↗

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

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