DURALOC 1220-32-452Recalls & reported problems
Depuy Orthopaedics, Inc. · DURALOC ACETABULAR CUP SYSTEM MARATHON POLYETHYLENE ACETABULAR LINER +4 OFFSET 32mm ID 52mm OD · Class 2 · Implant
All models of DURALOC (93)
Data updated Oct 18, 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 10603295015611), received between Jan 22, 2018 and Apr 3, 2026 — classified as 7 injuries.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
- Device Dislodged or Dislocated3
- Insufficient Device Problem Information1
Patient problems
- Joint Dislocation4
- No Code Available2
- Pain2
- Hypersensitivity/Allergic reaction1
- Joint Laxity1
- Unspecified Infection1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT HIP WAS SUBLUXATING. THE CUP REVISION WAS DONE AND REMOVED FEMORAL HEAD, REMOVED CUP AND LINER, REPLACED WITH EMPHASYS DUAL MOBILITY. DOI: (B)(6) 2019. DOR: (B)(6) 2026. AFFECTED SIDE: LEFT.
Patient problems: Joint Laxity
MAUDE report 24781837 ↗InjuryJan 5, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THE CUP WAS REVISED DUE TO DISLOCATION AND THERE WAS NO SURGICAL DELAY.
Patient problems: Joint Dislocation
MAUDE report 18458995 ↗InjuryFeb 23, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED TO ADDRESS HIP PAIN. DOI: UNKNOWN, DOR: (B)(6) 2021, AFFECTED SIDE: LEFT HIP.
Patient problems: Pain
MAUDE report 11366884 ↗InjuryFeb 25, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT DURALOC SHELL/ LINER AND SROM STEM/ HEAD WERE REMOVED FOR INFECTION AND CHRONIC DISLOCATION. STEM AND SHELL IMPLANTATION DATE ARE UNKNOWN. DOI: (B)(6) 2019. DOR: (B)(6) 2020, LEFT HIP.
Patient problems: Joint Dislocation; No Code Available; Unspecified Infection
MAUDE report 9749958 ↗InjuryNov 14, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SURGEON HAD TO REVISE THIS PRIMARY HIP DONE IN 2008. TAPER CORROSION. PSEUDO TUMOR.
Patient problems: Hypersensitivity/Allergic reaction; No Code Available
MAUDE report 9323537 ↗InjuryAug 14, 2018Insufficient Device Problem Information; Insufficient Device Problem Information
THE PATIENT WAS REVISED TO ADDRESS PAINFUL HIP DUE TO CHRONIC DISLOCATION. DOI: UNKNOWN; DOR: (B)(6) 2018; RIGHT HIP.
Patient problems: Joint Dislocation; Pain
MAUDE report 7781962 ↗InjuryJan 22, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated
DER STATED THAT THE PATIENT IS A CHRONIC DISLOCATOR AND THE SURGEON ELECTED TO OPEN THE HIP SURGICALLY TO DETERMINE THE FAILURE MECHANISM. HE ELECTED TO EXCHANGE THE LINER AND HEAD TO A CONSTRAINED ACETABULAR CONSTRUCT. DOI: UNKNOWN; DOR: (B)(6) 2017; RIGHT HIP.
Patient problems: Joint Dislocation
MAUDE report 7209852 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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