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DURALOC 2220-36-460Recalls & reported problems

Depuy Orthopaedics, Inc. · DURALOC TRIAL LINER +4 NEUTRAL 36ID x 60/72OD · Class 1

All models of DURALOC (93)

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 10603295102625), received between Apr 4, 2019 and Apr 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1
  • Scratched Material1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionApr 4, 2019Detachment of Device or Device Component; Scratched Material; Detachment of Device or Device Component; Scratched Material

    IT WAS REPORTED THAT THE CENTER, METAL PIECE OF THE LINERS HAS CAME OUT. THIS DID NOT OCCUR DURING SURGERY, THEREFORE NO PIECES NEEDED TO BE RETRIEVED FROM THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8484080 ↗

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Sources and updates

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