DURALOC 1220-28-054Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER Neutral 28mm ID 54mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295015086), received between May 3, 2021 and Jan 13, 2026 — classified as 3 injuries.
The most frequently reported specific device problem is “Naturally Worn” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Naturally Worn2
- Device Dislodged or Dislocated1
Patient problems
- Insufficient Information1
- Joint Dislocation1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJan 13, 2026Naturally Worn
IT WAS REPORTED THAT THE SURGEON IS ORDERING A PATIENT SPECIFIC HIP-INLAY FOR A PLANNED REVISION BECAUSE OF NORMAL AND EXPECTED PE-WEAR ON AN UNKNOWN SIDE. THERE HAS BEEN NO ALLEGATION OF ANY PRODUCT DEFICIENCY. THE REVISION WILL TAKE PLACE IN ABOUT THREE TO SIX MONTHS. DOI: >10 YRS AGO.
Patient problems: Insufficient Information
MAUDE report 24058822 ↗InjuryJan 6, 2023Naturally Worn; Naturally Worn
PATIENT WAS REVISED DUE TO HIP PAIN / POLY WEAR. HEAD, LINER, AND LOCKING RING EXCHANGED. ORIGINAL DATE OF SURGERY UNKNOWN. BELIEVED TO BE ABOUT 15 YEARS AGO. THERE WAS NO SURGICAL DELAY. DOI: UNKNOWN. DOR: ON (B)(6) 2022. AFFECTED SIDE: RIGHT HIP.
Patient problems: Pain
MAUDE report 16111839 ↗InjuryMay 3, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED TO ADDRESS HIP DISLOCATION. NEW HEAD AND LINER. DOI: UNKNOWN DOR: (B)(6) 2021 AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 11765311 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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