DURALOC 1220-28-052Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER Neutral 28mm 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
- 6
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295015079), received between Feb 20, 2018 and Aug 27, 2026 — classified as 4 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated3
- Naturally Worn2
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- Joint Dislocation3
- No Clinical Signs, Symptoms or Conditions2
- Fall1
- No Code Available1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2026Naturally Worn
It was reported that after a surgical procedure it was observed that the device had wear and tear. Affected Side: Left Side. Reason why the product is not available: Implanted.Have patients or users been harmed? No.Was there a significant delay? No.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50476463 ↗MalfunctionJun 2, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT PATIENT UNDERWENT A RIGHT HIP PROCEDURE ON (B)(6) 2025. THE WRONG SIZE LOCKING RING WAS PACKED. ANOTHER LOCKING RING WAS USED. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A DELAY OF FIFTEEN MINUTES. THERE WAS NO PATIENT CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22126468 ↗InjurySep 18, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT CUP, LINER, AND HEAD REMOVED AND REVISED DUE TO RECURRENT DISLOCATION. ALL PARTS RETRIEVED. NO DELAY. NO ADVERSE REACTIONS. NO OTHER INFORMATION KNOWN. DOI: (B)(6) 2001. DOR: (B)(6) 2024. AFFECTED SIDE: RIGHT HIP.
Patient problems: Fall; Joint Dislocation
MAUDE report 20248137 ↗InjurySep 13, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
PPF, STICKER SHEETS AND IMPLANT RECORDS RECEIVED. PPF ALLEGES DISLOCATION. DOI: (B)(6) 2006. DOR: NONE REPORTED, LEFT HIP.
Patient problems: Joint Dislocation
MAUDE report 9025710 ↗InjuryNov 2, 2018Naturally Worn; Naturally Worn
THE PATIENT WAS REVISED TO ADDRESS WORN THROUGH POLYETHYLENE.
Patient problems: No Code Available
MAUDE report 8034053 ↗InjuryFeb 20, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED TO ADDRESS DISLOCATION. IT WAS FOUND THAT NO ABDUCTORS WERE PRESENT. DOI: 2009; DOR: (B)(6) 2018. RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 7283728 ↗
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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