DJO SURGICAL 931-32-750Recalls & reported problems
Encore Medical, L.P. · LINER/NON-HOODED-NEU, MP6, HXe-plus, 32mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00888912099462), received between Dec 6, 2017 and Apr 1, 2025 — classified as 9 injuries.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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 Available4
- Adverse Event Without Identified Device or Use Problem3
- Device Operates Differently Than Expected1
- Unstable1
Patient problems
- Unspecified Infection3
- No Information2
- Bone Fracture(s)1
- Hip Fracture1
- Implant Pain1
- Joint Dislocation1
- No Code Available1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryApr 1, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PATIENT HAD MULTIPLE DISLOCATIONS AND PERIPROSTHETIC FRACTURE.
Patient problems: Bone Fracture(s); Joint Dislocation
MAUDE report 21749011 ↗InjuryDec 7, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - MDR - FALL LOWER BODY COMPONENT/FRACTURE-SIGNIFICANT ADVERSE EVENT.
Patient problems: Hip Fracture
MAUDE report 18288871 ↗InjuryJun 26, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryAug 26, 2020Unstable
InjuryFeb 28, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO POSSIBLE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9769404 ↗InjuryNov 12, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - SURGEON CHANGED THE HEAD AND POLY LINER TO ADD STABILITY TO THE PATIENTS TOTAL HIP PROSTHESIS.
Patient problems: No Information
MAUDE report 9310739 ↗InjurySep 18, 2019Appropriate Device Problem Term/Code Not Available
InjuryJul 26, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO PROLONGED INFECTION ISSUES, SURGEON DECIDED THE BEST WAY TO TREAT THE INFECTION WAS TO REMOVE THE POLY INSERT AND CERAMIC HEAD.
Patient problems: Unspecified Infection
MAUDE report 8832937 ↗InjuryDec 6, 2017Device Operates Differently Than Expected
REVISION SURGERY - DUE TO LEG LENGTH DISCREPANCY.
Patient problems: No Information
MAUDE report 7086743 ↗
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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