DURALOC 1220-28-152Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER 10 DEGREES Lip 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
- 12
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 10603295015178), received between Aug 10, 2017 and Sep 18, 2026 — classified as 11 injuries, 1 malfunction.
The most frequently reported specific device problem is “Naturally Worn” (8 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 Worn8
- Adverse Event Without Identified Device or Use Problem2
- Appropriate Device Problem Term/Code Not Available1
- Device Dislodged or Dislocated1
Patient problems
- Insufficient Information6
- No Code Available4
- Joint Dislocation1
- No Information1
- Pain1
- Unspecified Infection1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
InjurySep 18, 2026Naturally Worn
It was reported that duraloc liner poly wear, taking out 52 lipped liner, 52 locking ring, 28 1.5 head. No information on when it was implanted. Allpieces were retrieved. No delay in case.Affected Side: Left.
Patient problems: Insufficient Information
MAUDE report 50819940 ↗InjuryJun 10, 2026Naturally Worn
IT WAS REPORTED THAT THE ITEMS EXPLANTED AND REPLACED DUE TO SUSPECTED POLY WEAR. DOI: (B)(6) 2002, DOR: (B)(6) 2026. AFFECTED SIDE: UNKNOWN.
Patient problems: Insufficient Information
MAUDE report 25458671 ↗InjuryMay 29, 2026Naturally Worn
IT WAS REPORTED THAT THERE WAS A LEFT PE WORN OUT, REVISION NEEDED.
Patient problems: Insufficient Information
MAUDE report 25330982 ↗InjuryMar 9, 2026Naturally Worn
IT WAS REPORTED THAT THERE WAS WORN PE.
Patient problems: Insufficient Information
MAUDE report 24544691 ↗InjuryMar 6, 2026Naturally Worn
IT WAS REPORTED THE RIGHT INLAY WAS WORN OUT. IT WAS NOTED THE PATIENT OUTCOME WAS FULLY RECOVERED.
Patient problems: Insufficient Information
MAUDE report 24533054 ↗InjuryJul 25, 2024Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THERE WAS GENERAL WEAR AND TEAR AND POLY WEAR. HEAD AND LINER WERE EXCHANGED. DOI: UNKNOWN. DOR: (B)(6) 2024. AFFECTED SIDE: UNKNOWN HIP.
Patient problems: Insufficient Information
MAUDE report 19827260 ↗InjuryOct 19, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED DUE TO INFECTION. DOI: (B)(6) 2001. DOR: (B)(6) 2021, AFFECTED SIDE: RIGHT HIP.
Patient problems: Unspecified Infection
MAUDE report 12656130 ↗InjuryJun 12, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED DUE TO PAIN. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN, DOR: (B)(6) 2020, LEFT HIP.
Patient problems: No Code Available; Pain
MAUDE report 10148702 ↗InjuryJun 1, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
TH PATIENT WAS REVISED TO ADDRESS DISLOCATION. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN. DOR: (B)(6) 2020. AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 10106479 ↗InjuryMar 24, 2020Naturally Worn; Naturally Worn
DURALOC LINER EXCHANGE DUE TO WEAR OF THE POLYETHYLENE LINER.
Patient problems: No Code Available
MAUDE report 9871442 ↗MalfunctionAug 9, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
InjuryAug 10, 2017Naturally Worn; Naturally Worn
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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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