DJO SURGICAL 931-36-252Recalls & reported problems
Encore Medical, L.P. · LINER, ACETABULAR, NON-HOODED, NEUTRAL, HXL/FMP, 36MM ID, MP7 · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00888912099509), received between Aug 12, 2015 and Aug 4, 2025 — classified as 11 injuries.
The most frequently reported specific device problem is “Unstable” (3 reports).
1 other recall cover devices cleared under the same FDA submission (K072154); they may or may not involve this specific model.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available3
- Unstable3
- Adverse Event Without Identified Device or Use Problem2
- Device Dislodged or Dislocated2
- Insufficient Device Problem Information1
- Loose or Intermittent Connection1
Patient problems
- Failure of Implant3
- No Code Available3
- Unspecified Infection3
- Bone Fracture(s)1
- Fall1
- Joint Dislocation1
- No Known Impact Or Consequence To Patient1
- Pain1
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
InjuryAug 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryApr 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO PATIENT FALL/FRACTURE.
Patient problems: Bone Fracture(s); Fall
MAUDE report 21886955 ↗InjuryAug 3, 2020Unstable
REVISION SURGERY - INSTABILITY. REMOVED AND REPLACED THE LINER AND HEAD.
Patient problems: Failure of Implant; No Code Available
MAUDE report 10355734 ↗InjuryJul 6, 2020Unstable
REVISION SURGERY - DUE TO JOINT INSTABILITY.
Patient problems: Failure of Implant; No Code Available
MAUDE report 10234338 ↗InjuryDec 7, 2019Appropriate Device Problem Term/Code Not Available
InjuryOct 11, 2019Appropriate Device Problem Term/Code Not Available
InjurySep 6, 2019Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available
InjuryMay 9, 2019Unstable
REVISION SURGERY - DUE TO INSTABILITY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8597265 ↗InjuryJul 11, 2017Loose or Intermittent Connection
REVISION SURGERY - DUE TO A LOOSE CUP; THE SURGEON EXCHANGED OUT THE HEAD AND REMOVED THE CUP. HE USED A DIFFERENT VENDOR TO REPLACE THE CUP.
Patient problems: Failure of Implant
MAUDE report 6703344 ↗InjuryFeb 11, 2016Device Dislodged or Dislocated
REVISION SURGERY - THE SURGEON PUT A GRAPH IN THE ACETABULAR CUP. DUE TO THE GRAPH SHREDDING AND CAUSING THE PATIENT TO DISLOCATE; THE SURGEON TOOK THE ACETABULAR OUT AND PUT IN ALL NEW PARTS.
Patient problems: No Code Available
MAUDE report 5431548 ↗InjuryAug 12, 2015Insufficient Device Problem Information
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 4997966 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K072154. One submission often covers many models, so check the product and lot details in each record.
- Z-1130-2014 · Feb 7, 2014 · TerminatedFMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell to replicate the kinematics of a natural hi
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page