DJO SURGICAL 932-36-750Recalls & reported problems
Encore Medical, L.P. · LINER 10 DEG HOODED-NEU, MP6, HXe-plus, 36mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00190446177975), received between Feb 7, 2019 and Feb 11, 2022 — classified as 9 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available5
- Adverse Event Without Identified Device or Use Problem1
- Detachment of Device or Device Component1
- Device Dislodged or Dislocated1
- Malposition of Device1
- Output Problem1
- Unstable1
Patient problems
- Unspecified Infection5
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Joint Dislocation1
- No Code Available1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryFeb 11, 2022Adverse Event Without Identified Device or Use Problem
REVISION SURGERY DUE TO INFECTION. REMOVED THE CUP, LINER AND HEAD.
Patient problems: Unspecified Infection
MAUDE report 13514935 ↗InjuryDec 23, 2021Appropriate Device Problem Term/Code Not Available
InjuryOct 4, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - REVISED TOTAL HEAD ARTHROPLASTY DUE TO LINER DISLOCATION.
Patient problems: Joint Dislocation
MAUDE report 12568934 ↗InjurySep 8, 2021Output Problem
REVISION SURGERY - PATIENT HAD METALOSIS. CUP AND STEM STAYED IN PATIENT. LINER AND HEAD WERE EXCHANGED.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 12439745 ↗InjuryNov 13, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO INFECTION, SURGEON DID AN IRRIGATION & DRAINAGE WITH LINER EXCHANGE.
Patient problems: Unspecified Infection
MAUDE report 10836321 ↗InjuryApr 15, 2020Appropriate Device Problem Term/Code Not Available
SECOND REVISION SURGERY - PATIENT HAD REVISION SURGERY ON 3/8 WHERE ONLY THE STEM AND HEAD WERE REPLACED. EXPRT REVISION STEM PUT IN W/ 36 + 4 HEAD. PATIENT PRESENTED TO HOSPITAL A WEEK LATER W/ INFECTION. REVISION SURGERY TO REPLACE THE POLY AND HEAD.
Patient problems: Unspecified Infection
MAUDE report 9963680 ↗InjuryDec 23, 2019Malposition of Device; Detachment of Device or Device Component
REVISION SURGERY - LINER DISSOCIATED FROM THE CUP AND ROTATED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9511011 ↗InjuryDec 10, 2019Unstable
REVISION SURGERY - INSTABILITY IN HIP. EXCHANGED OUT THE LINER AND HEAD.
Patient problems: No Code Available
MAUDE report 9444555 ↗InjuryFeb 7, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION IN HIP. THE SURGEON REMOVED AND REPLACED THE LINER AND HEAD, THEN ADDED A DELTA OPTION SLEEVE.
Patient problems: Unspecified Infection
MAUDE report 8317742 ↗
Other Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented devices
- DJO SURGICAL 942-01-40HEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented2 recalls23 reports
- Vivacit-E® 110031012Zimmer, Inc. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall33 reports
- G7® Dual Mobility Acetabular System 110024462Biomet Orthopedics, LLC · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall22 reports
- DJO SURGICAL 942-01-36HEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall5 reports
- DJO SURGICAL 942-01-36JEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall1 report
- DJO SURGICAL 942-01-32CEncore Medical, L.P. · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented1 recall0 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145150Biomet Orthopedics, LLC · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented46 reports
- TAPERLOC COMPLETE MICRO PRIMARY FEMORAL 51-106160Biomet Orthopedics, LLC · Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented35 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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