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ATTUNE 1513-12-160Recalls & reported problems

Depuy (Ireland) · ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 12X160MM · 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 10603295043584), received between May 3, 2019 and May 3, 2019 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • No Code Available1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryMay 3, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT HAS A HISTORY OF RECURRING INFECTION. THE DOCTORS BELIEVED THE INFECTION HAD BEEN ERADICATED AND WENT AHEAD WITH THE REIMPLANTATION. AFTER MULTIPLE WASHOUTS AND WOUND VAC CHANGES, SURGEON HAD TO REMOVE IMPLANTS AND PUT IN AN ANTIBIOTIC SPACER. DOI: (B)(6) 2019. DOR: (B)(6) 2019; LEFT KNEE.

    Patient problems: No Code Available; Unspecified Infection

    MAUDE report 8578828 ↗

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

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