DJO SURGICAL 400-32-000Recalls & reported problems
Encore Medical, L.P. · HEAD, FEMORAL 32/+0.0 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 8
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00888912076364), received between Sep 24, 2015 and May 29, 2026 — classified as 8 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
- Adverse Event Without Identified Device or Use Problem3
- Device Dislodged or Dislocated3
- Fracture1
- Insufficient Device Problem Information1
Patient problems
- No Code Available3
- Joint Dislocation2
- Bone Fracture(s)1
- Implant Pain1
- Insufficient Information1
- Unspecified Infection1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryMay 29, 2026Insufficient Device Problem Information
REVISION SURGERY DUE TO UNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 25330044 ↗InjuryJul 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PATIENT WAS EXPERIENCING DISCOMFORT WHEN EXTENDING THE OPERATIVE LEG.
Patient problems: Implant Pain
MAUDE report 22475286 ↗InjuryMar 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 10, 2019Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT PRESENTING WITH AN INFECTION. THE SURGEON PERFORMED AN IRRIGATION & DRAINAGE PROCEDURE AND SWAPPED THE HEAD & POLY. LOTS OF FLUID AND JOINT PUSS WHEN OPENED.
Patient problems: Unspecified Infection
MAUDE report 8236424 ↗InjuryAug 8, 2018Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT HAVING DISLOCATED.
Patient problems: No Code Available
MAUDE report 7765138 ↗InjuryJan 24, 2018Fracture
SECOND REVISION SURGERY - DUE TO THE PATIENT HAVING A PERIPROSTHETIC FEMUR FRACTURE. THE SURGEON REMOVED AND REPLACED THE ORIGINAL STEM AND HEAD.
Patient problems: Bone Fracture(s); No Code Available
MAUDE report 7217032 ↗InjuryDec 22, 2015Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT'S TOTAL HIP HAVING DISLOCATED.
Patient problems: Joint Dislocation
MAUDE report 5319956 ↗InjurySep 24, 2015Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE THE PATIENT DISLOCATING THEIR HIP. THE SURGEON CHANGED OUT THE ORIGINAL HEAD AND LINER.
Patient problems: No Code Available
MAUDE report 5101063 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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