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ATTUNE 1506-00-001Recalls & reported problems

Depuy (Ireland) · ATTUNE KNEE SYSTEM TIBIAL BASE FIXED BEARING SIZE 1 CEMENTED · Class 2 · Implant

All models of ATTUNE (1475)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295042358), received between Jan 30, 2019 and Jan 30, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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

  • Loss of or Failure to Bond1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryJan 30, 2019Loss of or Failure to Bond; Loss of or Failure to Bond

    PATIENT WAS REVISED DUE TO THE TIBIA LIKELY LOOSENING AS THE CEMENT WAS LEFT ENTIRELY ON THE TIBIA, COMPLETELY SEPARATING FROM THE PROSTHESIS.

    Patient problems: No Code Available

    MAUDE report 8288789 ↗

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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