DURALOC 1220-32-158Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER 10 DEGREES Lip 32mm ID 58 or 70mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10603295015567), received between Aug 20, 2018 and Jul 28, 2026 — classified as 10 injuries.
The most frequently reported specific device problem is “Naturally Worn” (8 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 Worn8
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
Patient problems
- Insufficient Information5
- No Clinical Signs, Symptoms or Conditions2
- Joint Dislocation1
- Not Applicable1
- Pain1
- Unspecified Infection1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryJul 28, 2026Naturally Worn
It was reported that the patient experienced polyethylene wear of the left inlay.
Patient problems: Insufficient Information
MAUDE report 50061157 ↗InjuryMar 4, 2026Naturally Worn
IT WAS REPORTED THAT THE PATIENT EXPERIENCED THE WEAR OR DETERIORATION OF POLYETHYLENE MATERIAL IN THE RIGHT HIP IMPLANT, WITH NO PATIENT HARM. THE REVISION SURGERY DATE IS NOT KNOWN AT THIS STAGE AS THE CUSTOM-MADE PRODUCT NEEDS TO BE MANUFACTURED FIRST.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24513931 ↗InjuryFeb 18, 2026Naturally Worn
SURGEON IS ORDERING A PATIENT SPECIFIC HIP-INLAY FOR A PLANNED REVISION BECAUSE OF NORMAL AND EXPECTED PE-WEAR LEFT SIDE. DOI: >10 YRS AGO. DOR: PLANNED TO TAKE PLACE AS SOON AS POSSIBLE. THERE HAS BEEN NO ALLEGATION OF ANY PRODUCT DEFICIENCY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24380483 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE RIGHT SIDE. REVISION SURGERY IS NEEDED. ORIGINAL IMPLANT DATE: (B)(6) 2006.
Patient problems: Insufficient Information
MAUDE report 23536220 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE RIGHT SIDE. REVISION SURGERY IS NEEDED. ORIGINAL IMPLANT DATE: (B)(6) 2005.
Patient problems: Insufficient Information
MAUDE report 23536046 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE RIGHT SIDE. REVISION SURGERY IS NEEDED; WILL TAKE PLACE WHEN NEW IMPLANT IS RECEIVED.
Patient problems: Insufficient Information
MAUDE report 23535199 ↗InjurySep 12, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT UNDERWENT DURALOCK POLY EXCHANGE DUE TO WEAR AND METAL HEAD EXCHANGE. AFFECTED SIDE: LEFT HIP.
Patient problems: Insufficient Information
MAUDE report 23040305 ↗InjuryNov 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED DUE TO ACUTE INFECTION. ORIGINAL IMPLANT DATE UNKNOWN. NO SURGICAL DELAY. DOI: UNKNOWN; DOR: (B)(6) 2021; AFFECTED SIDE: UNKNOWN.
Patient problems: Unspecified Infection
MAUDE report 12777904 ↗InjurySep 4, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED TO ADDRESS CHRONIC DISLOCATION. DOI: UNKNOWN; DOR: (B)(6) 2018; RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 7841751 ↗InjuryAug 20, 2018Naturally Worn; Naturally Worn
THE PATIENT WAS REVISED TO ADDRESS PAINFUL HIP DUE TO POLY WEAR. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN. DOR: (B)(6) 2018. RIGHT HIP.
Patient problems: Not Applicable; Pain
MAUDE report 7796831 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 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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