DURALOC 1220-32-152Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER 10 DEGREES Lip 32mm ID 52mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy Duraloc hip liner is a plastic cup insert used in hip replacement. Reports mostly describe the liner wearing out after years of use and needing revision surgery, with a few hip dislocations. There are 26 reports naming its identifier, mentioning 26 injuries and no deaths. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 29
- Deaths reported
- 0
- Injuries reported
- 28
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 29 adverse event reports that list this exact device (DI 10603295015536), received between Dec 12, 2017 and Sep 16, 2026 — classified as 28 injuries, 1 malfunction.
The most frequently reported specific device problem is “Naturally Worn” (19 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 Worn19
- Device Dislodged or Dislocated6
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- Insufficient Information11
- No Code Available8
- Joint Dislocation6
- No Clinical Signs, Symptoms or Conditions3
- Pain3
- Injury1
- Joint Laxity1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 25 most recent of 29 reports, in the reporter's own words as published by the FDA.
InjurySep 16, 2026Naturally Worn
Patient problems: Insufficient Information
MAUDE report 50795302 ↗InjurySep 16, 2026Naturally Worn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795178 ↗MalfunctionSep 11, 2026Naturally Worn
It was reported that a worn-out left insert had been observed. The issue related to polyethylene wear associated with long-term use and not to the locking ring itself. All available information has been disclosed.
Patient problems: Insufficient Information
MAUDE report 50736840 ↗InjuryMar 31, 2026Device Dislodged or Dislocated
IT WAS REPORTED THAT PATIENT EXPERIENCED A CHRONIC DISLOCATION OF OPERATIVE HIP. PATIENT UNDERWENT AN ACETABULUM REVISION. DOI- (B)(6) 2020. DOR- (B)(6) 2026. AFFECTED SIDE-RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 24745006 ↗InjuryFeb 10, 2026Naturally Worn
ADDITIONAL INFORMATION RECEIVED: B. WAS THERE ANY ADVERSE CONSEQUENCE TO THE PATIENT RELEVANT TO THIS EVENT? IF YES, PLEASE KINDLY PROVIDE DETAILS. -> NO ADVERSE CONSEQUENCES. C. PLEASE PROVIDE THE EXACT ALLEGATION OF REPORTED PRODUCTS. -> INLAY: WEAR. -> LOCKING RING: NO ALLEGATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24303013 ↗InjuryJan 29, 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 UNKNOWN SIDE. THERE HAS BEEN NO ALLEGATION OF ANY PRODUCT DEFICIENCY. DOI: >10 YRS AGO. DOR: PLANNED TO TAKE PLACE AS SOON AS POSSIBLE.
Patient problems: Insufficient Information
MAUDE report 24210208 ↗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) 2005.
Patient problems: Insufficient Information
MAUDE report 23536369 ↗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 23534756 ↗InjuryNov 3, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED A REVISION SURGERY OCCURRED BECAUSE THE LEFT HIP DURALOC MARATHON ACETABULAR LINER AND LOCKING RING ARE WORN OUT. ORIGINAL IMPLANT DATE WAS (B)(6) 2010
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23452604 ↗InjuryOct 28, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THERE WAS A WORN OUT DURALOC MARATHON HIP IMPLANT-RIGHT SIDE. REVISION SURGERY IS NEEDED.
Patient problems: Insufficient Information
MAUDE report 23406355 ↗InjuryOct 28, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THERE WAS WORN OUT DURALOC MARATHON IMPLANT. REVISION SURGERY IS NEEDED.
Patient problems: Insufficient Information
MAUDE report 23406245 ↗InjuryJul 10, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT WAS SHOWING SIGNS OF POLY WEAR, SO THE SURGEON REVISED THE LINER AND HEAD BALL. THERE WAS NO DELAY IN SURGERY. NO KNOWN INFECTION PRESENT. THE ORIGINAL SURGICAL DATE IS NOT KNOWN. DOI: UNKNOWN, DOR: (B)(6) 2025, AFFECTED SIDE: RIGHT HIP.
Patient problems: Insufficient Information
MAUDE report 22474803 ↗InjuryJun 26, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT HAD A WORN OUT PE ON THE RIGHT HIP JOINT. REVISION SURGERY IS NEEDED.
Patient problems: Insufficient Information
MAUDE report 22337838 ↗InjuryJun 26, 2025Naturally Worn; Naturally Worn
ADDITIONAL INFORMATION WAS RECEIVED AND STATES THAT A. WAS/WERE THERE ANY PATIENT CONSEQUENCE/S RELATED TO THE EVENT? NO. B. CAN YOU CONFIRM THE PRIMARY SURGERY DATE OR THE ORIGINAL IMPLANTATION DATE? UNKNOWN. C. WHAT WAS THE EFFECTED SIDE? LEFT OR RIGHT? RIGHT. D. IS THERE ANY DATE SCHEDULED FOR THE REVISION SURGERY DUE TO THE REPORTED EVENT? NOT FIXED YET.
Patient problems: Insufficient Information
MAUDE report 22335614 ↗InjuryMay 19, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PE INSERT IS WORN OUT AND REVISION SURGERY IS NEEDED.
Patient problems: Insufficient Information
MAUDE report 22043837 ↗InjuryMar 7, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO DISLOCATION. IT WAS UNKNOWN IF THERE WAS A SURGICAL DELAY. AFFECTED SIDE: LEFT HIP.
Patient problems: Joint Dislocation
MAUDE report 21546992 ↗InjuryMar 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO INSTABILITY. NO SURGICAL DELAY. DOI: (B)(6) 2023. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Laxity
MAUDE report 16637055 ↗InjurySep 16, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE CUP REVISION AND REPLACEMENT OF RECLAIM PROXIMAL BODY DUE TO DISLOCATION. DURALOC CUP WAS REMOVED AND REPLACED WITH A COMPETITOR DUAL MOBILITY CONSTRUCT. THE RECLAIM PROXIMAL BODY WAS REMOVED AND REPLACED WITH A NEW ONE WITH DIFFERENT RETROVERSION. THERE WAS NO SURGICAL DELAY OR PATIENT HARM. DOI: (B)(6) 2022. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 15439462 ↗InjuryAug 30, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO INFECTION. NO SURGICAL DELAY WAS REPORTED. DOI: UNKNOWN. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT HIP.
Patient problems: Unspecified Infection
MAUDE report 15323970 ↗InjurySep 11, 2020Naturally Worn; Naturally Worn
IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO POLY WEAR. DOI: (B)(6) 2001. DOR: (B)(6) 2020. AFFECTED SIDE: RIGHT HIP.
Patient problems: No Code Available
MAUDE report 10523344 ↗InjuryJul 6, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED DUE TO PAINFUL HIP. REMOVED CUP, HEAD, LINER AND REVISED TO DEPUY MULTIHOLE CUP, HEAD AND LINER. ORIGINAL IMPLANT DATE IS UNKNOWN SO IS ORIGINAL HOSPITAL. DOI: UNKNOWN, DOR: (B)(6) 2020, AFFECTED SIDE: LEFT HIP.
Patient problems: No Code Available; Pain
MAUDE report 10236141 ↗InjuryMar 9, 2020Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT HAD A PREVIOUS TOTAL HIP REPLACEMENT WITH A DURALOC CUP AND LARGE TAPER STEM. SURGEON REPLACED THE DURALOC LINER BECAUSE OF POLY WEAR AND THE LARGE TAPER HEAD BALL. DOI: UNKNOWN, DOR: (B)(6) 2020, AFFECTED SIDE: LEFT SIDE.
Patient problems: No Code Available
MAUDE report 9806792 ↗InjuryJan 17, 2020Naturally Worn; Naturally Worn
FAILED ACETABULUM LEFT HIP. POLY WEAR.
Patient problems: No Code Available; Pain
MAUDE report 9603759 ↗InjuryJan 17, 2020Naturally Worn; Naturally Worn
PATIENT WAS REVISED TO ADDRESS WORN POLY. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN; DOR: (B)(6) 2020; RIGHT HIP.
Patient problems: No Code Available
MAUDE report 9601904 ↗InjuryApr 18, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT HAD HEAD REPLACED AND REMOVAL OF DURALOC CUP/LINER. REVISED WITH STRYKER MDM CUP. DOI: UNKNOWN, DOR: (B)(6) 2019, UNKNOWN AFFECTED SIDE.
Patient problems: Injury; No Code Available; Osteolysis; Pain
MAUDE report 8528344 ↗
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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