DJO SURGICAL 932-40-756Recalls & reported problems
Encore Medical, L.P. · LINER 10 DEG HOODED-NEU, MP9, HXE-PLUS, 40MM · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 15
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00888912100335), received between Sep 3, 2015 and Apr 3, 2026 — classified as 15 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 Problem7
- Appropriate Device Problem Term/Code Not Available5
- Loose or Intermittent Connection2
- Insufficient Device Problem Information1
- Unstable1
Patient problems
- Unspecified Infection8
- Pain4
- Loss of Range of Motion2
- Bone Fracture(s)1
- Failure of Implant1
- Insufficient Information1
- Joint Dislocation1
- No Information1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem
PATIENT EXPERIENCED A PERIPROSTHETIC FRACTURE AND WAS POSSIBLY INFECTED. THE LINER WAS THEREFORE CHANGED.
Patient problems: Bone Fracture(s); Unspecified Infection
MAUDE report 24780626 ↗InjuryOct 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryNov 7, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMar 31, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMar 23, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 10, 2022Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY: DUE TO LOOSENING OF INSERT.
Patient problems: Insufficient Information
MAUDE report 14346372 ↗InjuryJan 25, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAS PERSISTENT PAIN AFTER PRIMARY HIP RECONSTRUCTION. SURGEON DECIDED TO TAKE THE PATIENT BACK AND REVISE THE ACETABULAR.
Patient problems: Pain
MAUDE report 11225179 ↗InjuryAug 21, 2020Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO INFECTION, INCISION & DRAINAGE. INSERT AND HEAD EXCHANGED, PAIN AND LOSS OF MOTION.
Patient problems: Loss of Range of Motion; Pain; Unspecified Infection
MAUDE report 10436809 ↗InjuryJun 2, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO PAIN AND LOSS OF MOTION.
Patient problems: Loss of Range of Motion; Pain
MAUDE report 10112764 ↗InjuryMay 28, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAD INFECTION. SURGEON REMOVED HEAD/LINER, DID A COMPLETE WASH OUT AND THEN REPLACED WITH NEW IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 10096598 ↗InjuryJan 21, 2020Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9611237 ↗InjuryOct 16, 2019Loose or Intermittent Connection
InjuryAug 23, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAD INFECTION AND NEEDED A WASH OUT AND REPLACEMENT OF THE HEAD, LINER AND SLEEVE.
Patient problems: Unspecified Infection
MAUDE report 8928338 ↗InjuryFeb 22, 2016Unstable
REVISION SURGERY - DUE TO THE PATIENT'S HIP BEING UNSTABLE; THE SURGEON REMOVED ALL OF THE ORIGINAL IMPLANTS EXCEPT THE STEM AND CUP.
Patient problems: No Information
MAUDE report 5451182 ↗InjurySep 3, 2015Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT HAVING PAIN IN GROIN AREA.
Patient problems: Pain
MAUDE report 5053733 ↗
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 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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