DURALOC 1220-28-056Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER Neutral 28mm ID 56 or 68mm 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
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295015093), received between Apr 11, 2018 and Nov 29, 2022 — classified as 7 injuries.
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.
Most reported problems
Device problems
- Naturally Worn4
- Adverse Event Without Identified Device or Use Problem2
- Device Dislodged or Dislocated1
Patient problems
- No Code Available4
- Pain4
- Discomfort1
- Joint Dislocation1
- Not Applicable1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryNov 29, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO PAIN. DOI: UNKNOWN. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT HIP.
Patient problems: Pain
MAUDE report 15877472 ↗InjuryAug 24, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT EXPERIENCED MULTIPLE DISLOCATIONS. DOI: UNKNOWN; DOR: (B)(6) 2022; AFFECTED SIDE: UNKNOWN.
Patient problems: Joint Dislocation
MAUDE report 15289782 ↗InjuryOct 15, 2020Naturally Worn; Naturally Worn
IT WAS REPORTED AS PAIN DUE TO A WORN POLY LINER. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN, DOR: (B)(6) 2020, AFFECTED SIDE: RIGHT HIP.
Patient problems: No Code Available; Pain
MAUDE report 10683403 ↗InjuryJul 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
LEFT TOTAL HIP REVISION. PATIENT REPORTING THIGH PAIN. REVISED STEM, FEMORAL HEAD, AND POLY LINER.
Patient problems: No Code Available; Pain
MAUDE report 10296076 ↗InjuryJul 14, 2020Naturally Worn; Naturally Worn
ADDITIONAL INFORMATION RECEIVED STATED THAT THE PATIENT WAS REVISED DUE TO MILD HIP DISCOMFORT. OPERATIVE SIDE IS RIGHT.
Patient problems: Discomfort; No Code Available; Pain
MAUDE report 10270970 ↗InjuryJul 31, 2018Naturally Worn; Naturally Worn
IT WAS REPORTED THAT POLY AND HEAD EXCHANGED DUE TO POLY WEAR. DOI: (B)(6) 2000; DOR: (B)(6) 2018; RIGHT HIP.
Patient problems: No Code Available
MAUDE report 7734705 ↗InjuryApr 11, 2018Naturally Worn; Naturally Worn
DER STATES POLY WEAR. DOI: UNKNOWN, DOR:(B)(6) 2018, UNKNOWN AFFECTED SIDE.
Patient problems: Not Applicable
MAUDE report 7421670 ↗
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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