DJO SURGICAL 932-32-250Recalls & reported problems
Encore Medical, L.P. · LINER, ACETABULAR, HOODED, NEUTRAL, 10°, HXL/FMP, 32MM ID, MP6 · 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 00888912100038), received between Feb 8, 2017 and Apr 20, 2022 — classified as 7 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (4 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.
Most reported problems
Device problems
- Device Dislodged or Dislocated4
- Adverse Event Without Identified Device or Use Problem2
- Appropriate Device Problem Term/Code Not Available1
- Naturally Worn1
Patient problems
- No Code Available4
- Joint Dislocation2
- Fall1
- Insufficient Information1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryApr 20, 2022Naturally Worn; Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT COMPLAINT OF HIP CLICKING. POLY LINER WAS WORN THROUGH AT THE SUPERIOR-POSTERIOR 1/3 MARGIN OF THE LINER. THE CUP WAS ORIGINALLY PLACED IN A VERY VERTICAL POSITION AS INDICATED ON X-RAY. METAL HEAD WAS ALSO REMOVED WITH SOME MINOR SCUFFING OF THE SURFACE.
Patient problems: Insufficient Information
MAUDE report 14160860 ↗InjuryMay 16, 2018Device Dislodged or Dislocated
REPORTED INCIDENT - DUE TO CHRONIC DISLOCATION. THE SURGEON PERFORMED A CLOSED REDUCTION. NO IMPLANTS WERE REMOVED.
Patient problems: No Code Available
MAUDE report 7520156 ↗InjuryMay 16, 2018Device Dislodged or Dislocated
REPORTED INCIDENT - DUE TO CHRONIC DISLOCATION. THE SURGEON PERFORMED A CLOSED REDUCTION. NO IMPLANTS WERE REMOVED.
Patient problems: No Code Available
MAUDE report 7520068 ↗InjuryMay 16, 2018Adverse Event Without Identified Device or Use Problem
REPORTED INCIDENT - DUE TO CHRONIC DISLOCATION. THE SURGEON PERFORMED A CLOSED REDUCTION. NO IMPLANTS WERE REMOVED.
Patient problems: No Code Available
MAUDE report 7520048 ↗InjuryMay 16, 2018Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT HAVING CHRONIC DISLOCATION.
Patient problems: No Code Available
MAUDE report 7519933 ↗InjuryFeb 16, 2017Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO THE PATIENT FALLING AND DISLOCATING, THE SURGEON NEEDED TO PERFORM A REVISION SURGERY.
Patient problems: Fall; Joint Dislocation
MAUDE report 6337497 ↗InjuryFeb 8, 2017Device Dislodged or Dislocated
REVISION SURGERY - DUE TO DISLOCATION OF THE HIP.
Patient problems: Joint Dislocation
MAUDE report 6312992 ↗
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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