DJO SURGICAL 932-36-752Recalls & reported problems
Encore Medical, L.P. · LINER 10 DEG. HOODED NEU, MP7, HXe-plus, 36mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 20
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 20 adverse event reports that list this exact device (DI 00888912100168), received between Dec 6, 2018 and May 27, 2025 — classified as 20 injuries.
The most frequently reported specific device problem is “Corroded” (1 report).
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
- Appropriate Device Problem Term/Code Not Available9
- Adverse Event Without Identified Device or Use Problem8
- Corroded1
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
- Therapeutic or Diagnostic Output Failure1
- Unstable1
Patient problems
- Unspecified Infection11
- Pain3
- Joint Dislocation2
- Medical device site infection2
- No Code Available2
- Insufficient Information1
- Loss of Range of Motion1
Recent adverse event reports
The 20 most recent of 20 reports, in the reporter's own words as published by the FDA.
InjuryMay 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryDec 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 19, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO DISLOCATION AND INFECTION.
Patient problems: Joint Dislocation; Unspecified Infection
MAUDE report 19785601 ↗InjuryOct 20, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - LOCKING BOLT BROKE.
Patient problems: Insufficient Information
MAUDE report 17981434 ↗InjuryDec 30, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO AN INFECTION WASH OUT HEAD AND POLY SWAP.
Patient problems: Medical device site infection
MAUDE report 16077591 ↗InjuryNov 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Medical device site infection
MAUDE report 15801389 ↗InjuryJul 13, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - THE PATIENT WAS COMPLAINING ABOUT PAIN. THE X-RAY LOOKED PERFECT, SO THE SURGEON REPLACED THE LINER AND PUT A NEW DELTA OPTION HEAD IN WITH SLEEVE.
Patient problems: Pain
MAUDE report 12159669 ↗InjuryJan 5, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PAINFUL, LOSS OF MOTION.
Patient problems: Loss of Range of Motion; Pain
MAUDE report 11120430 ↗InjuryDec 4, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT WAS INFECTED.
Patient problems: Unspecified Infection
MAUDE report 10949855 ↗InjuryNov 16, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 10843861 ↗InjurySep 11, 2020Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO INFECTION. REMOVED AND REPLACED THE HEAD AND LINER.
Patient problems: Unspecified Infection
MAUDE report 10523289 ↗InjuryJan 10, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - IRRIGATION AND DRAINAGE WASHOUT FOR INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9574660 ↗InjuryNov 1, 2019Appropriate Device Problem Term/Code Not Available
InjurySep 18, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT DISLOCATED - LINER SWAP.
Patient problems: Joint Dislocation
MAUDE report 9085006 ↗InjuryJul 26, 2019Unstable; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - REVISED THE TOTAL HIP FOR INSTABILITY AND PAIN.
Patient problems: Pain
MAUDE report 8833660 ↗InjuryMay 2, 2019Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT'S HIP BEING INFECTED AND ALL COMPONENTS NEEDED TO BE REMOVED.
Patient problems: Unspecified Infection
MAUDE report 8574460 ↗InjuryApr 16, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8520128 ↗InjuryMar 15, 2019Corroded; Therapeutic or Diagnostic Output Failure
REVISION SURGERY - DUE TO SEVERE METALLOSIS. IT APPEARS THAT THE HEAD WAS RUBBING AGAINST THE INTERIOR OF THE CUP CAUSING THE LINER TO FAIL. IT WAS A SUCCESSFUL REVISION OF THE ACETABULAR COMPONENT (HEAD, LINER, SHELL, AND SCREWS).
Patient problems: No Code Available
MAUDE report 8424767 ↗InjuryJan 22, 2019Insufficient Device Problem Information
REVISION SURGERY - DUE TO A SUPERFICIAL INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8267020 ↗InjuryDec 6, 2018Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT HAVING DISLOCATED. THE SURGEON EXCHANGED LINER FOR A CONSTRAINED LINER.
Patient problems: No Code Available
MAUDE report 8139893 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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