DURALOC 1220-32-160Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER 10 DEGREES Lip 32mm ID 60 or 72mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295015574), received between Jan 5, 2018 and Oct 28, 2025 — classified as 5 injuries.
The most frequently reported specific device problem is “Naturally Worn” (3 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 Worn3
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
Patient problems
- No Code Available2
- Insufficient Information1
- Joint Dislocation1
- Joint Laxity1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryOct 28, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THERE WAS A WORN OUT PE ON THE RIGHT HIP JOINT. REVISION SURGERY IS NEEDED.
Patient problems: Insufficient Information
MAUDE report 23401951 ↗InjuryJul 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT HAD BECOME UNSTABLE AND UNDERWENT REVISION TO GET STABILITY. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED FOR REPORTING. NO FURTHER INFORMATION WAS PROVIDED. DOI: (B)(6) 2002, DOR: (B)(6) 2025, AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Laxity
MAUDE report 22420858 ↗InjuryAug 27, 2019Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT HAD POLY WEAR SINCE 2000. DOI: UNKNOWN. DOR: (B)(6) 2019, LEFT HIP.
Patient problems: No Code Available
MAUDE report 8935172 ↗InjurySep 27, 2018Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE ACETABULAR LINER WAS REPLACED DUE TO NORMAL WEAR.
Patient problems: No Code Available
MAUDE report 7915628 ↗InjuryJan 5, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT WAS REVISED TO ADDRESS DISLOCATION. THE SURGEON WENT IN AND REMOVED THE STANDARD 10 DEG INSERT AND REPLACED IT WITH A CONSTRAINED INSERT. HE ALSO CHANGED THE INTERNAL POLY LOCKING RING. THE HEAD WAS REPLACED WITH A TS CERAMIC HEAD, 32 + 5. THE STEM AND CUP WERE WELL FIXED AND RETAINED. DOI: (B)(6) 2017; DOR: (B)(6) 2017; LEFT HIP.
Patient problems: Joint Dislocation
MAUDE report 7168270 ↗
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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