DJO SURGICAL 411-00-145Recalls & reported problems
Encore Medical, L.P. · HEAD, UNIPOLAR, MODULAR, ENCORE SIZE45 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888912076807), received between Sep 8, 2015 and Sep 30, 2026 — classified as 5 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
- Appropriate Device Problem Term/Code Not Available2
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
- Insufficient Device Problem Information1
Patient problems
- Unspecified Infection3
- Joint Dislocation1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Joint Dislocation
MAUDE report 50941455 ↗InjuryJul 13, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO INFECTION WASH OUT AND HEAD CHANGE.
Patient problems: Unspecified Infection
MAUDE report 15001933 ↗InjuryJul 5, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO INFECTION WASH OUT.
Patient problems: Unspecified Infection
MAUDE report 14921088 ↗InjuryMay 31, 2019Fracture
REVISION SURGERY - DUE TO THE PATIENT HAVING A PERIPROSTHETIC FRACTURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8659682 ↗InjurySep 8, 2015Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION. THE SURGEON EXCHANGED THE UNIPOLAR AND SLEEVE.
Patient problems: Unspecified Infection
MAUDE report 5060589 ↗
Other Prosthesis, Hip, Hemi-, Femoral, Metal devices
- UHR UH1-48-28Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal2 recalls3 reports
- "UNITED" USTAR II Knee System 2515-3111United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3213United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- STAGEONE 431207Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3115United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- ACTIS 101011050Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal73 reports
- UHR UH1-46-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
- UHR UH1-45-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 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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