DJO SURGICAL 932-36-754Recalls & reported problems
Encore Medical, L.P. · LINER 10 DEG. HOODED NEU, MP8 HXE-PLUS, 36MM · Class 2 · Implant
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 15
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00888912100175), received between Aug 12, 2016 and Mar 19, 2026 — classified as 15 injuries.
The most frequently reported specific device problem is “Contamination” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available7
- Adverse Event Without Identified Device or Use Problem6
- Contamination1
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
Patient problems
- Unspecified Infection10
- Insufficient Information2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Joint Laxity1
- No Code Available1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2026Adverse Event Without Identified Device or Use Problem
InjuryOct 24, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryFeb 29, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 20, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 25, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 14498303 ↗InjuryFeb 11, 2022Appropriate Device Problem Term/Code Not Available
InjuryMar 11, 2021Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - PATIENT HAD SEVERE HETROTOPIC OSSIFICATION DEVELOP POST-OPERATION. LINER WAS ONLY REMOVED TO DO A THROUGH WASHOUT OF THE SURGICAL SITE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11461788 ↗InjuryFeb 4, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - INDEX SURGERY PERFORMED APPROXIMATELY 3 YEARS AGO. PATIENT WAS TAKEN TO SURGERY FOR IRRIGATION AND DRAINAGE OF RIGHT TOTAL HIP WITH HEAD AND LINER EXCHANGE. IDENTICAL SIZE COMPONENTS WERE IMPLANTED ( BIOLOX OPTION HEAD WAS USED).
Patient problems: Insufficient Information
MAUDE report 11278946 ↗InjurySep 5, 2020Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO DISLOCATION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10498119 ↗InjuryAug 28, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - INFECTION, PATIENT NEEDED AN IRRIGATION AND DRAINAGE WITH A HEAD BALL/LINER SWAP OUT.
Patient problems: Unspecified Infection
MAUDE report 10466854 ↗InjuryMay 29, 2020Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - THE PATIENT WAS INFECTED. SO THE SURGEON JUST DID A WASH OUT AND REPLACED THE 2 IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 10101313 ↗InjuryMar 12, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - INCISION AND DRAIN, INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9825936 ↗InjuryJan 4, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8218124 ↗InjuryDec 11, 2017Contamination
REVISION SURGERY - DUE TO AN INFECTION. THE SURGEON DID A POLY EXCHANGE.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 7105031 ↗InjuryAug 12, 2016Insufficient Device Problem Information
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 5873499 ↗
Other Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented devices
- DJO SURGICAL 942-01-40HEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented2 recalls23 reports
- Vivacit-E® 110031012Zimmer, Inc. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall33 reports
- G7® Dual Mobility Acetabular System 110024462Biomet Orthopedics, LLC · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall22 reports
- DJO SURGICAL 942-01-36HEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall5 reports
- DJO SURGICAL 942-01-36JEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall1 report
- DJO SURGICAL 942-01-32CEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall0 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145150Biomet Orthopedics, LLC · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented46 reports
- TAPERLOC COMPLETE MICRO PRIMARY FEMORAL 51-106160Biomet Orthopedics, LLC · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented35 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.