DJO SURGICAL 931-36-750Recalls & reported problems
Encore Medical, L.P. · LINER/NON-HOODED-NEU, MP6, HXe-plus, 36mm · Class 2 · Implant
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 00190446177913), received between May 13, 2019 and Dec 29, 2023 — classified as 13 injuries.
The most frequently reported specific device problem is “Unstable” (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 Available9
- Adverse Event Without Identified Device or Use Problem4
- Unstable1
Patient problems
- Unspecified Infection10
- Bone Fracture(s)1
- Fall1
- 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.
InjuryDec 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 28, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMar 23, 2021Adverse Event Without Identified Device or Use Problem
InjuryDec 4, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTED HIP. SWAPPED THE HEADBALL AND THE LINER AFTER CLEANING OUT THE JOINT.
Patient problems: Unspecified Infection
MAUDE report 10945103 ↗InjurySep 18, 2020Appropriate Device Problem Term/Code Not Available
SECOND REVISION SURGERY - PATIENT DEVELOPED AN INFECTION. SURGEON OPTED TO REMOVE EVERYTHING AND DO AN IRRIGATION AND DRAINAGE AND REPLACE WITH NEW IMPLANTS.
Patient problems: Unspecified Infection
MAUDE report 10553707 ↗InjurySep 1, 2020Appropriate Device Problem Term/Code Not Available
InjuryApr 11, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAD INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9951629 ↗InjuryFeb 27, 2020Appropriate Device Problem Term/Code Not Available
InjuryFeb 12, 2020Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - PATIENT HAD INFECTION.
Patient problems: Unspecified Infection
MAUDE report 9700560 ↗InjuryJul 15, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT FELL AND FRACTURED HER LEG.
Patient problems: Bone Fracture(s); Fall
MAUDE report 8791265 ↗InjuryJun 21, 2019Unstable; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO INSTABILITY. SURGEON REMOVED THE STEM, HEAD AND LINER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8724388 ↗InjuryJun 7, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT HAVING PRESENTED ONE MONTH POST OP WITH AN INFECTION. THE SURGEON PERFORMED AN IRRIGATION & DRAINAGE AND REPLACED THE HEAD AND LINER.
Patient problems: Unspecified Infection
MAUDE report 8680523 ↗InjuryMay 13, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION. THE SURGEON DID AN IRRIGATION AND DEBRIDEMENT (I&D).
Patient problems: Unspecified Infection
MAUDE report 8605014 ↗
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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