DURALOC 1220-32-156Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER 10 DEGREES Lip 32mm ID 56 or 68mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 19
- Deaths reported
- 0
- Injuries reported
- 19
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 19 adverse event reports that list this exact device (DI 10603295015550), received between Sep 7, 2017 and Mar 4, 2026 — classified as 19 injuries.
The most frequently reported specific device problem is “Naturally Worn” (14 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Naturally Worn14
- Device Dislodged or Dislocated4
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Insufficient Information13
- Joint Dislocation4
- No Code Available2
- Pain1
- Unspecified Infection1
Recent adverse event reports
The 19 most recent of 19 reports, in the reporter's own words as published by the FDA.
InjuryMar 4, 2026Naturally Worn
IT WAS REPORTED THAT THE PATIENT EXPERIENCED THE WEAR OR DETERIORATION OF POLYETHYLENE MATERIAL IN THE LET 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: Insufficient Information
MAUDE report 24513648 ↗InjuryFeb 19, 2026Naturally Worn
IT WAS REPORTED THAT DUR MAR 10D LNR 32IDX56OD EXPERIENCED WEAR OR DETERIORATION OF THE POLYETHYLENE MATERIAL IN A HIP IMPLANT ON THE LEFT SIDE, RESULTING IN THE NEED FOR REVISION SURGERY. THE IMPLANT WAS PLACED DURING A SURGERY IN 2004, AND THE COMPLAINT DEVICE REMAINS IMPLANTED. IT WAS NOTED THAT THERE IS SOME UNCERTAINTY AS TO WHETHER THE WORN IMPLANT IS A DURALOC MARATHON OR ENDURON, DUE TO THE TIME ELAPSED SINCE THE ORIGINAL PROCEDURE.
Patient problems: Insufficient Information
MAUDE report 24387952 ↗InjuryJan 22, 2026Naturally Worn
SURGEON IS ORDERING A PATIENT SPECIFIC HIP-INLAY FOR A PLANNED REVISION BECAUSE OF NORMAL AND EXPECTED PE-WEAR UNKNOWN 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: Insufficient Information
MAUDE report 24144264 ↗InjuryJan 9, 2026Naturally Worn
IT WAS REPORTED THAT THE DURALOC MARATHON HIP IMPLANT ON THE LEFT SIDE WAS WORN OUT. REVISION SURGERY IS NEEDED. THE REVISION SURGERY DATE IS NOT KNOWN AT THIS STAGE AS THE CUSTOM-MADE PRODUCT NEEDS TO BE MANUFACTURED FIRST.
Patient problems: Insufficient Information
MAUDE report 24023314 ↗InjuryDec 10, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THE SURGEON IS ORDERING A PATIENT SPECIFIC HIP-INLAY FOR A PLANNED REVISION BECAUSE OF NORMAL AND EXPECTED PE-WEAR UNKNOWN SIDE. DOI: UNKNOWN >10 YRS. AGO. DOR: UNKNOWN PLANNED TO TAKE PLACE IN 2026.
Patient problems: Insufficient Information
MAUDE report 23769419 ↗InjuryNov 13, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE RIGHT SIDE. REVISION SURGERY IS NEEDED.
Patient problems: Insufficient Information
MAUDE report 23544630 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE LEFT SIDE. REVISION SURGERY IS NEEDED. ORIGINAL IMPLANT DATE: (B)(6) 2006.
Patient problems: Insufficient Information
MAUDE report 23536310 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE RIGHT SIDE. REVISION SURGERY IS NEEDED; WILL BE PERFORMED WHEN NEW IMPLANT IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 23536122 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE LEFT SIDE. REVISION SURGERY IS NEEDED; WILL BE PERFORMED WHEN NEW IMPLANT IS PROVIDED.
Patient problems: Insufficient Information
MAUDE report 23535515 ↗InjuryNov 12, 2025Naturally Worn; Naturally Worn
WORN OUT DURALOC MARATHON HIP IMPLANT ON THE LEFT SIDE. REVISION SURGERY IS NEEDED; WILL BE PERFORMED WHEN NEW IMPLANT IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 23535350 ↗InjuryNov 5, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT WAS IN PAIN. THERE WAS A WORN OUT DURALOC MARATHON HIP IMPLANT-LEFT SIDE. REVISION SURGERY IS NEEDED.
Patient problems: Pain
MAUDE report 23475446 ↗InjuryOct 28, 2025Naturally Worn; Naturally Worn
ADDITIONAL INFORMATION RECEIVED: WAS THERE A SURGICAL DELAY? IF YES, WHAT IS THE DURATION OF THE DELAY? THERE WAS NO SURGERY YET, PATIENT IS WAITING FOR THE NEW IMPLANT.
Patient problems: Insufficient Information
MAUDE report 23406272 ↗InjuryAug 22, 2024Naturally Worn; Naturally Worn
IT WAS REPORTED, THAT THE POLY WAS WORN AND FEMORAL HEAD WERE EXPLANTED. DOI: UNKNOWN, DOR: (B)(6) 2024, AFFECTED SIDE: LEFT FEMUR.
Patient problems: Insufficient Information
MAUDE report 20032884 ↗InjuryMay 11, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION WAS RECEIVED AND STATED THAT THE AFFECTED SIDE WAS THE RIGHT HIP. NO PATIENT CONSEQUENCES WERE REPORTED.
Patient problems: Unspecified Infection
MAUDE report 16914474 ↗InjuryJul 6, 2021Naturally Worn; Naturally Worn
IT WAS STATED THAT PATIENT WAS REVISED DUE TO WORN POLY. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN - DOR: (B)(6) 2021 (RIGHT HIP).
Patient problems: Insufficient Information
MAUDE report 12123058 ↗InjuryApr 23, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED DUE TO DISLOCATION. DOI: UNKNOWN. DOR: (B)(6) 2020; RIGHT HIP.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 9991465 ↗InjuryOct 10, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT WAS DISLOCATING.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 7951024 ↗InjuryOct 27, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated
COMPLAINT DESCRIPTION: PATIENT WAS REVISED TO ADDRESS MULTIPLE DISLOCATIONS. SURGEON WANTED TO REMOVE CUP AND LINER AND PLACE WITH NEW DUAL MOBILITY SYSTEM. TO HELP WITH THE DISLOCATION THE CUP LINER WERE REMOVED AND A NEW HEAD WAS PLACED ON STEM.
Patient problems: Joint Dislocation
MAUDE report 6984396 ↗InjurySep 7, 2017Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED TO ADDRESS RECURRENT DISLOCATION AND LOOSENING OF THE COMPETITOR STEM.
Patient problems: Joint Dislocation
MAUDE report 6849057 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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