DURALOC 1220-28-050Recalls & reported problems
Depuy Orthopaedics, Inc. · Duraloc MARATHON ACETABULAR LINER Neutral 28mm ID 50mm 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
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295015062), received between Apr 20, 2018 and Apr 21, 2026 — classified as 6 injuries.
The most frequently reported specific device problem is “Naturally Worn” (5 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 Worn5
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
Patient problems
- Joint Laxity2
- Insufficient Information1
- Joint Dislocation1
- Joint Disorder1
- No Code Available1
- No Consequences Or Impact To Patient1
- Not Applicable1
- Pain1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryApr 21, 2026Naturally Worn
IT WAS REPORTED THAT SWITCHED OUT DURALOC LINER AND DYNAMIC RING LOCK RETAINED THE EXISTING HEAD. LINER HAD ECCENTRIC WEAR.
Patient problems: Insufficient Information
MAUDE report 24936565 ↗InjuryJul 28, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT REVISED DUE TO DISLOCATING POSTERIORLY. THE SURGEON DECIDED TO REMOVE THE HEAD, LINER AND CUP TO CEMENT IN A BIMENTUM CUP FOR MORE STABILITY. UPON TRIALING HE DETERMINED HE NEED MORE LENGTH AND ELECTED TO GO WITH A 28 +15.5 HEAD. HE WAS NOTIFIED THAT THIS HEAD HAD A SKIRT AND SHOULDN¿T BE USED WITH THIS CONSTRUCT AND WANTED TO PROCEED IN USING IT. NO FURTHER PATIENT INFORMATION IS AVAILABLE AT THIS TIME. DOI: UNKNOWN; DOR: (B)(6) 2022; AFFECTED SIDE: RIGHT HIP.
Patient problems: Joint Dislocation; Joint Laxity
MAUDE report 15121728 ↗InjuryAug 24, 2021Naturally Worn; Adverse Event Without Identified Device or Use Problem; Naturally Worn; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE CUP WAS REMOVED DUE TO MALPOSITION. THE HEAD HAD WORN THE POLY DOWN OVER TIME.
Patient problems: Joint Laxity
MAUDE report 12362683 ↗InjuryNov 29, 2018Naturally Worn; Naturally Worn
THE PATIENT WAS REVISED TO ADDRESS PAIN DUE TO WORN POLY.
Patient problems: No Code Available; Pain
MAUDE report 8115622 ↗InjuryAug 24, 2018Naturally Worn; Naturally Worn
PATIENT HAD ECCENTRIC WEAR OF THE POLY LINER SO THE HIP FELT UNSTABLE.
Patient problems: Joint Disorder
MAUDE report 7812484 ↗InjuryApr 20, 2018Naturally Worn; Naturally Worn
DER STATES THAT THE PATIENT HAD THR MANY YEARS AGO. DATE AND HOSPITAL UNKNOWN. SURGEON REVISED DUE TO POLYWEAR. DOI: UNKNOWN; DOR: (B)(6) 2018; LEFT HIP.
Patient problems: No Consequences Or Impact To Patient; Not Applicable
MAUDE report 7446341 ↗
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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