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DURALOC 1220-28-060Recalls & reported problems

Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER Neutral 28mm ID 60 or 72mm OD · Class 2 · Implant

All models of DURALOC (93)

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 10603295015116), received between Mar 1, 2019 and Mar 1, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Naturally Worn” (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

  • Naturally Worn1

Patient problems

  • Joint Disorder1
  • 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.

  • InjuryMar 1, 2019Naturally Worn; Naturally Worn

    PATIENT WAS REVISED TO ADDRESS POLY WEAR AFTER 19 YEARS WHICH LED TO INSTABILITY.

    Patient problems: Joint Disorder; No Code Available

    MAUDE report 8381728 ↗

Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices

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Sources and updates

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