DJO SURGICAL 932-36-756Recalls & reported problems
Djo, LLC · LINER 10 DEG 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 00888912100182), received between Dec 5, 2016 and Jan 18, 2024 — classified as 13 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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
- Appropriate Device Problem Term/Code Not Available5
- Adverse Event Without Identified Device or Use Problem4
- Device Dislodged or Dislocated3
- Loose or Intermittent Connection1
- Positioning Problem1
Patient problems
- Unspecified Infection7
- Fall2
- Insufficient Information2
- No Information1
- No Known Impact Or Consequence To Patient1
- Wound Dehiscence1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
InjuryJan 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO POSSIBLE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 16153490 ↗InjuryFeb 8, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT FELL AND THE WOUND OPENED UP.
Patient problems: Fall; Wound Dehiscence
MAUDE report 13479959 ↗InjuryJan 6, 2022Positioning Problem
COMPLAINT - DUE TO LINER NOT SEATING CORRECTLY.
Patient problems: Insufficient Information
MAUDE report 13173658 ↗InjuryOct 21, 2021Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY : PATIENT PRESENTED WITH A LOOSENED FEMORAL STEM. THE ORIGINAL LINER WAS REMOVED TO REPLACE THE STEM, NEW LINER WAS REPLACED.
Patient problems: Insufficient Information
MAUDE report 12678262 ↗InjuryJan 13, 2021Device Dislodged or Dislocated
REVISION SURGERY - PATIENT FELL DAYS AFTER INITIAL SURGERY. HIP WAS DISLOCATING, SO A CONSTRAINING LINER WAS NEEDED.
Patient problems: Fall
MAUDE report 11163278 ↗InjuryApr 24, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - SURGEON DID A LINER AND HEAD SWAP ON THE PATIENT DUE TO POSSIBLE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9995737 ↗InjuryDec 6, 2019Appropriate Device Problem Term/Code Not Available
InjuryMay 24, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN THE PATIENT HAVING AN INFECTION. THE SURGEON WASHED OUT THE JOINT AND SWAPPED THE CERAMIC HEAD AND POLY LINER.
Patient problems: Unspecified Infection
MAUDE report 8639975 ↗InjuryMar 8, 2019Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT HAVING DISLOCATED HIS HIP.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8404562 ↗InjuryJun 27, 2018Device Dislodged or Dislocated
REVISION SURGERY - DUE TO CHRONIC DISLOCATION.
Patient problems: No Information
MAUDE report 7642926 ↗InjuryMar 1, 2018Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO AN IRRIGATION AND DRAINAGE FOR INFECTION. THE SURGEON SWAPPED THE HEAD AND POLY.
Patient problems: Unspecified Infection
MAUDE report 7307825 ↗InjuryDec 5, 2016Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT GETTING AN INFECTION AFTER SURGERY; THE SURGEON WASHED OUT THE JOINT AND REPLACED THE POLY AND HEAD.
Patient problems: Unspecified Infection
MAUDE report 6145510 ↗
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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