DJO SURGICAL 931-36-760Recalls & reported problems
Djo, LLC · LINER/NON-HOODED-NEU, MP10, HXe-plus, 36mm · Class 2 · Implant
All models of DJO SURGICAL (42)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 13
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00888912099646), received between Sep 7, 2016 and Jun 22, 2026 — classified as 13 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 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 Problem5
- Appropriate Device Problem Term/Code Not Available4
- Insufficient Device Problem Information2
- Patient Device Interaction Problem1
- Patient-Device Incompatibility1
Patient problems
- Unspecified Infection10
- Discomfort1
- Implant Pain1
- Inflammation1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
InjuryJun 22, 2026Patient Device Interaction Problem
REVISION SURGERY - DUE TO HAS PAIN ASSOCIATED WITH EXTERNAL ROTATION AND ABDUCTION OF THE HIP.
Patient problems: Implant Pain
MAUDE report 25586570 ↗InjuryJun 28, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PERI-PROSTHETIC JOINT INFECTION 2 WEEKS POST OPERATION. INCISION AND DEBRIDEMENT WITH POLY AND FEMORAL HEAD EXCHANGE.
Patient problems: Unspecified Infection
MAUDE report 12080882 ↗InjuryJan 10, 2020Adverse Event Without Identified Device or Use Problem
InjuryOct 15, 2019Appropriate Device Problem Term/Code Not Available
InjurySep 25, 2019Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - PATIENT HAD INFECTION ON FOOT THAT SPREAD TO HIP JOINT.
Patient problems: Unspecified Infection
MAUDE report 9120369 ↗InjuryAug 16, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PERI-PROSTHETIC INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8903657 ↗InjuryJun 5, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT'S HIP BECOMING UNSTABLE. THE SURGEON PUT IN A CONSTRAINED LINER AND CHANGED THE HEAD.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8671081 ↗InjuryApr 1, 2019Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT DEVELOPING AN INFECTION. THE STEM, HEAD, AND LINER WERE REMOVED, WASHED OUT, AND NEW COMPONENTS WERE PUT IN.
Patient problems: Unspecified Infection
MAUDE report 8469411 ↗InjuryFeb 20, 2018Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 7284194 ↗InjuryJul 17, 2017Patient-Device Incompatibility
REVISION SURGERY - DUE TO THE PATIENT PRESENTING TO THE SURGEON WITH A SUSPICIOUS INFLAMED SCAR ON HIS HIP. AFTER ASPIRATION OF THE HIP JOINT THE DOCTOR OF RECORD ORDERED AN IRRIGATION AND DEBRIDEMENT PROCEDURE AND PLANNED TO REMOVE THE HEAD AND LINER THEN REPLACE WITH NEW IMPLANTS. THE SURGEON FOLLOWED THE SAME INCISION FROM THE PREVIOUS SURGERY TO EXPOSE THE HIP JOINT. HE THEN SWABBED FOR CULTURES AND REMOVED THE HEAD THEN LINER. HE REPLACED THE HEAD AND LINER WITH NEW IMPLANTS. THE HEAD WAS A STRYKER ORTHOPEDIC PRODUCT AND THE LINER FROM (B)(4). THE PATIENT WAS THEN CLOSED
Patient problems: Inflammation
MAUDE report 6718794 ↗InjuryFeb 14, 2017Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO A HIP INFECTION IN PATIENT.
Patient problems: Unspecified Infection
MAUDE report 6330150 ↗InjuryJan 16, 2017Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 6254698 ↗InjurySep 7, 2016Insufficient Device Problem Information
REVISION SURGERY - THE PATIENT PRESENTED AT DOCTORS OFFICE WITH DISCOMFORT. PATIENT WAS SCHEDULED FOR A WASHOUT OF WOUND AND DURING SURGERY IT WAS DETERMINED THE INFECTION WAS NOT JUST SUPERFICIAL; IT INVOLVED THE JOINT CAPSULE. THE SURGEON DECIDED TO DO A HEAD AND LINER EXCHANGE WITH WASH OUT. EXPLANTS WERE IN GOOD CONDITION.
Patient problems: Discomfort; Unspecified Infection
MAUDE report 5934542 ↗
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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page