DJO SURGICAL 932-36-252Recalls & reported problems
Encore Medical, L.P. · LINER, ACETABULAR, HOODED, NEUTRAL, 10°, HXL/FMP, 36MM ID, MP7 · Class 2 · Implant
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00888912100076), received between Jan 20, 2017 and Sep 3, 2024 — classified as 9 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available4
- Device Dislodged or Dislocated3
- Adverse Event Without Identified Device or Use Problem2
- Fracture1
Patient problems
- Failure of Implant3
- Joint Dislocation2
- Implant Pain1
- Joint Disorder1
- Joint Laxity1
- No Code Available1
- No Known Impact Or Consequence To Patient1
- Unspecified Infection1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjurySep 3, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PATIENT PRESENTED WITH HIP PAIN. SURGEON ELECTED TO DO A HEAD AND LINER SWAP OUT.
Patient problems: Implant Pain
MAUDE report 20131615 ↗InjurySep 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - REMOVAL OF ALL HEAD AND LINER DUE TO UNSTABLE HIP.
Patient problems: Joint Laxity
MAUDE report 15432726 ↗InjuryJul 3, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DURING POST-OPERATION X-RAY, FOREIGN DEBRIS WAS NOTICED. SURGEON DID A WASH OUT AND REMOVED DEBRIS AND EXCHANGED IMPLANTS.
Patient problems: No Code Available
MAUDE report 10229725 ↗InjuryMay 19, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 10071257 ↗InjuryJan 21, 2020Device Dislodged or Dislocated
REVISION SURGERY - DUE TO A POST-OP DISLOCATION.
Patient problems: Failure of Implant; Joint Disorder
MAUDE report 9611236 ↗InjuryNov 6, 2019Device Dislodged or Dislocated
REVISION SURGERY - DUE TO DISLOCATION.
Patient problems: Failure of Implant; Joint Dislocation
MAUDE report 9285997 ↗InjuryJun 18, 2019Fracture; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT HAVING A PERIPROSTHETIC HIP FRACTURE. THE SURGEON REMOVED THE ORIGINAL STEM AND HEAD AND WENT TO A REVISION HIP SYSTEM. HE REPLACED THE ORIGINAL 10 DEGREE LINER WITH A 20 DEGREE LINER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8709891 ↗InjuryMay 1, 2018Device Dislodged or Dislocated
InjuryJan 20, 2017Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT DISLOCATING.
Patient problems: Joint Dislocation
MAUDE report 6266580 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.