DURALOC 1220-32-052Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER Neutral 32mm ID 52mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295015451), received between Jul 19, 2018 and Nov 3, 2025 — classified as 6 injuries, 1 malfunction.
The most frequently reported specific device problem is “Naturally Worn” (4 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 Worn4
- Device Dislodged or Dislocated2
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Pain3
- Insufficient Information2
- Joint Dislocation2
- No Code Available2
- Not Applicable1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 3, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THERE IS A POLY WEAR OF DURALOC HIP LINER WITH NO REPORTED INTERVENTION OR TREATMENT AT THIS TIME.
Patient problems: Insufficient Information
MAUDE report 23452312 ↗InjuryJun 6, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SURGEON ORDERED A PATIENT SPECIFIC HIP-INLAY FOR A PLANNED REVISION BECAUSE OF NORMAL AND EXPECTED PE-WEAR ON THE LEFT SIDE. REVISION WAS SCHEDULED.
Patient problems: Insufficient Information
MAUDE report 22157478 ↗InjuryJul 25, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED WITH ACETABULAR REVISION DUE TO CHRONIC DISLOCATION. THERE WAS NO REPORTED LOOSENING. THERE WAS NO REPORTED SURGICAL DELAY. DOI: (B)(6), 2022. DOR: (B)(6), 2022. AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 15095090 ↗InjuryFeb 21, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
A PATIENT WAS TREATED WITH A BIOLOX FORTE CERAMIC FEMORAL HEAD. AS THE PATIENT WAS TURNED ON TO THE BACK POST SURGERY THE FEMORAL HEAD DISENGAGED AND HAD TO BE REVISED.
Patient problems: Joint Dislocation; No Code Available; Not Applicable
MAUDE report 9738675 ↗InjuryMay 8, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION DUE TO PAIN. DOI: UNK, DOR: (B)(6) 2019, LEFT HIP.
Patient problems: No Code Available; Pain
MAUDE report 8591186 ↗InjuryDec 14, 2018Naturally Worn; Appropriate Device Problem Term/Code Not Available; Naturally Worn; Appropriate Device Problem Term/Code Not Available
InjuryJul 19, 2018Naturally Worn; Naturally Worn
THE PATIENT WAS REVISED TO ADDRESS PAINFUL HIP DUE TO WORN POLY. DOI: UNKNOWN; DOR: (B)(6) 2018; RIGHT HIP.
Patient problems: Pain
MAUDE report 7704371 ↗
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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