DJO SURGICAL 931-36-756Recalls & reported problems
Djo, LLC · LINER/NON-HOODED-NEU, MP9, 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 00888912099639), received between Jul 6, 2017 and Oct 16, 2025 — classified as 13 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 Available8
- Adverse Event Without Identified Device or Use Problem5
- Device Dislodged or Dislocated1
Patient problems
- Unspecified Infection9
- Extraskeletal ossification1
- Implant Pain1
- Insufficient Information1
- No Code Available1
- 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.
InjuryOct 16, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT HETEROTOPIC OSSIFICATION OCCURRED. A NEW LINER AND HEAD WERE IMPLANTED. THE PART NUMBER FOR THE HEAD WAS UNRECOGNIZABLE, SO IT COULD NOT BE IDENTIFIED.
Patient problems: Extraskeletal ossification
MAUDE report 23319299 ↗InjuryJun 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PAIN AND INFECTION.
Patient problems: Implant Pain; Unspecified Infection
MAUDE report 17122129 ↗InjuryApr 4, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 16, 2022Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT DISLOCATED. SURGEON REPLACED A 36 NEUTRAL LINER AND 36 HEAD.
Patient problems: Insufficient Information
MAUDE report 13262909 ↗InjuryDec 29, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAD A POSSIBLE INFECTION, WASHED THE WOUND AND DID A HEAD AND LINER SWAP.
Patient problems: Unspecified Infection
MAUDE report 11087238 ↗InjuryOct 21, 2019Appropriate Device Problem Term/Code Not Available
InjurySep 27, 2019Appropriate Device Problem Term/Code Not Available
InjurySep 26, 2019Appropriate Device Problem Term/Code Not Available
InjuryAug 27, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - REVISED FOR INSTABILITY. SWAPPED THE HEAD AND LINER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8937486 ↗InjuryJul 3, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO POSSIBLE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8759629 ↗InjuryApr 22, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8535967 ↗InjuryMar 5, 2018Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - THE SURGEON WASHED THE JOINT AND REPLACED THE IMPLANTS WITH NEW ONES.
Patient problems: No Code Available
MAUDE report 7314201 ↗InjuryJul 6, 2017Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT HAVING A HIP INFECTION.
Patient problems: Unspecified Infection
MAUDE report 6691773 ↗
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.
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