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ATTUNE 1504-11-223Recalls & reported problems

Depuy (Ireland) · ATTUNE FEMORAL POROCOAT POSTERIOR STABILIZED SIZE 3N RIGHT CEMENTLESS · 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 10603295042105), received between Sep 22, 2020 and Sep 22, 2020 — 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.

  • InjurySep 22, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    CLINICAL ADVERSE EVENT RECEIVED FOR CHEST X-RAY RESULT RIGHT LOWER ZONE MEDICALLY. TREAT AS A RESPIRATORY TRACT INFECTION. EVENT IS NOT SERIOUS AND IS CONSIDERED MILD EVENT IS DEFINITELY NOT RELATED TO DEVICE AND IS POSSIBLY RELATED TO PROCEDURE. DATE OF IMPLANTATION: (B)(6) 2020 DATE OF EVENT (ONSET): (B)(6) 2020 (RIGHT KNEE). TREATMENT: COMMENCED ON IV ANTIBIOTICS RECOVERED/RESOLVED: (B)(6) 2020.

    Patient problems: No Code Available; Unspecified Infection

    MAUDE report 10567777 ↗

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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