DJO SURGICAL 495-00-075Recalls & reported problems
Encore Medical, L.P. · EXPRT Revision Hip, Standard Offset Proximal Body, 75mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 14
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 00190446153825), received between Feb 12, 2018 and Oct 24, 2025 — classified as 14 injuries.
The most frequently reported specific device problem is “Unstable” (3 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem5
- Appropriate Device Problem Term/Code Not Available4
- Unstable3
- Device Dislodged or Dislocated1
- Difficult to Remove1
- Positioning Problem1
Patient problems
- Joint Dislocation5
- Joint Laxity4
- Fall3
- No Code Available2
- Unspecified Infection2
- Limb Fracture1
- Pain1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
InjuryOct 24, 2025Unstable; Unstable
InjuryJun 23, 2025Unstable; Adverse Event Without Identified Device or Use Problem; Unstable; Adverse Event Without Identified Device or Use Problem
InjuryJun 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - DUE TO DISLOCATION AND LOOSENING.
Patient problems: Joint Dislocation; Joint Laxity
MAUDE report 22181163 ↗InjuryJan 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 26, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY DUE TO LOOSENING, IMPLANT SHIFTED.
Patient problems: Joint Laxity
MAUDE report 16251006 ↗InjuryJun 3, 2022Appropriate Device Problem Term/Code Not Available
REVISION SURGERY DUE TO PATIENT SUBSIDING.
Patient problems: Joint Dislocation
MAUDE report 14598604 ↗InjuryOct 4, 2021Appropriate Device Problem Term/Code Not Available
InjurySep 27, 2021Positioning Problem
REVISION SURGERY - THE PATIENT FELL AND THE CUFF WAS DISPLACED. CUFF LINER AND SCREWS WERE ALL TAKEN OUT.
Patient problems: Fall
MAUDE report 12532662 ↗InjuryApr 1, 2021Difficult to Remove
REVISION SURGERY - THE PATIENT FELL AS AT THE NURSING HOME AND FRACTURED THEIR FEMUR. SURGEON PLATED THE FEMUR. HE THEN TRIED TO GET THE EXPRT TOTAL HIP ARTHROPLASTY OUT BUT WAS NOT ABLE TO SO HE HAD TO CUT THE NECK OFF WITH A METAL CUTTING BURR.
Patient problems: Fall; Limb Fracture
MAUDE report 11605147 ↗InjuryJun 2, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT WAS UNSTABLE AND HAS PAIN FROM A FALL.
Patient problems: Fall; Pain
MAUDE report 10108749 ↗InjuryOct 16, 2019Appropriate Device Problem Term/Code Not Available
SECOND REVISION SURGERY - PATIENT ACQUIRED POST-OPERATIVE INFECTION. SURGEON PERFORMED A WASH OUT, PULLED ALL POLY CUP AND CHANGED PROXIMAL BODY WITH A BIPOLAR HEAD THIS TIME.
Patient problems: Unspecified Infection
MAUDE report 9197680 ↗InjuryJan 14, 2019Unstable
REVISION SURGERY - AFTER SPEAKING WITH THE PATIENT, THE SURGEON DECIDED TO EXCHANGE THE 75 STANDARD OFFSET PROXIMAL BODY WITH A 85 LATERAL OFFSET TO CREAT MORE STABILITY FOR THE PATIENT.
Patient problems: No Code Available
MAUDE report 8244992 ↗InjuryApr 30, 2018Adverse Event Without Identified Device or Use Problem
SECOND REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION. THE PATIENT HAD A REVISION TOTAL HIP ARTHROPLASTY (THA) PERFORMED PREVIOUSLY, WHICH BECAME INFECTED. THE SURGEON PERFORMED AN INCISION AND DRAINAGE (I&D) ALONG WITH A HEAD, LINER, AND PROXIMAL BODY EXCHANGE.
Patient problems: Unspecified Infection
MAUDE report 7473955 ↗InjuryFeb 12, 2018Device Dislodged or Dislocated
REVISION SURGERY - DUE TO THE PATIENT HAVING DISLOCATED.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 7263314 ↗
Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 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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