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ATTUNE 1504-00-223Recalls & reported problems

Depuy (Ireland) · ATTUNE KNEE SYSTEM FEMORAL CRUCIATE RETAINING NARROW SIZE 3N RIGHT CEMENTED · Class 3 · Implant

All models of ATTUNE (1475)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 10603295041269), received between Mar 12, 2021 and Mar 12, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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 16, 2026.

Most reported problems

Device problems

  • Device Contaminated During Manufacture or Shipping1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMar 12, 2021Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping

    IT WAS REPORTED THAT ATTUNE FEMORAL RIGHT IMPLANT WAS OPENED AND RESIDUE WAS ON POSTERIOR FEMORAL CONDYLE. THE IMPLANT WAS REMOVED FROM SURGICAL FIELD AND A NEW IMPLANT WAS OPENED. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11477573 ↗

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Sources and updates

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