DJO SURGICAL 931-40-754Recalls & reported problems
Encore Medical, L.P. · LINER/NON-HOODED-NEU, MP8, HXe-plus, 40mm · Class 2 · Implant
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 00190446177920), received between Aug 8, 2018 and Dec 28, 2021 — classified as 7 injuries.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available7
- Patient-Device Incompatibility1
Patient problems
- Unspecified Infection4
- Insufficient Information1
- No Code Available1
- No Known Impact Or Consequence To Patient1
- Pain1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryDec 28, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO INFECTION, TRIED A NEW POLY.
Patient problems: Unspecified Infection
MAUDE report 13095986 ↗InjuryMay 28, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY- THE LINER WAS NOT PROPERLY SEATED DOWN IN THE FIRST CASE, SO IT DISENGAGED. THEREFORE, THE LINER WAS REMOVED AND REPLACED. LINER WAS SEATED PROPERLY INTO THE CUP.
Patient problems: Insufficient Information
MAUDE report 11901603 ↗InjuryJan 12, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - EXCHANGED HEAD AND LINER DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 11155574 ↗InjuryAug 2, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - IRRIGATION & DRAINAGE POLY SWAP.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8855386 ↗InjuryJan 10, 2019Appropriate Device Problem Term/Code Not Available
SECOND REVISION SURGERY - DUE TO THE PATIENT HAVING A POST OP INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8236558 ↗InjuryJan 4, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT HAVING A POST OP INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8218197 ↗InjuryAug 8, 2018Patient-Device Incompatibility; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT REPORTING PAIN. THE SURGEON CHANGED OUT THE SHELL, LINER, AND HEAD.
Patient problems: No Code Available; Pain
MAUDE report 7763036 ↗
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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