DJO SURGICAL 932-44-760Recalls & reported problems
Encore Medical, L.P. · LINER 10 DEG HOODED-NEU, MP10, HXe-plus, 44mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00888912100472), received between Aug 31, 2016 and Apr 7, 2026 — classified as 7 injuries.
The most frequently reported specific device problem is “Fracture” (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
- Adverse Event Without Identified Device or Use Problem3
- Appropriate Device Problem Term/Code Not Available3
- Fracture1
- Unstable1
Patient problems
- Unspecified Infection3
- Medical device site infection2
- Bone Fracture(s)1
- Fall1
- Joint Dislocation1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryApr 7, 2026Unstable
A PATIENT WITH FMP CUP WAS DISLOCATING SO DOCTOR CONSTRAINED THEM.
Patient problems: Joint Dislocation
MAUDE report 24811568 ↗InjuryNov 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - PATIENT HAD INFECTION, IT WAS CLEANED AND WASHOUT.
Patient problems: Medical device site infection
MAUDE report 15801433 ↗InjuryNov 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY DUE TO AN INFECTION, CLEAN AND WASHOUT.
Patient problems: Medical device site infection
MAUDE report 15801314 ↗InjurySep 22, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - THE PATIENT PRESENTED WITH SIGNS OF INFECTION, THE SURGEON WENT INTENDING TO WASH OUT AND DEBRIDE AND ULTIMATELY DECIDED TO REMOVE COMPONENTS SO THE INFECTION COULD RESIDE AND HE WOULD REVISE THE HIP AT A LATER DATE.
Patient problems: Unspecified Infection
MAUDE report 10568409 ↗InjuryMar 19, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - INFECTION, WASH OUT.
Patient problems: Unspecified Infection
MAUDE report 9854013 ↗InjuryJul 8, 2019Fracture; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAD FALLEN OFF HIS BIKE AND HAD A PERIPROSTHETIC FRACTURE. REMOVED EVERYTHING EXCEPT THE CUP AND SCREWS.
Patient problems: Bone Fracture(s); Fall
MAUDE report 8768376 ↗InjuryAug 31, 2016Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 5919607 ↗
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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