DJO SURGICAL 495-01-075Recalls & reported problems
Encore Medical, L.P. · EXPRT Revision Hip, Lateral Offset Proximal Body, 75mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00190446153856), received between Oct 27, 2017 and Aug 13, 2026 — classified as 10 injuries.
The most frequently reported specific device problem is “Unstable” (2 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 Available2
- Unstable2
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information3
- Joint Laxity3
- Unspecified Infection2
- Bone Fracture(s)1
- No Code Available1
- Pain1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryAug 13, 2026Unstable
Patient problems: Joint Laxity
MAUDE report 50230338 ↗InjuryAug 13, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - COMPLETED A PROXIMAL BODY REPLACEMENT AND CONSTRAINED LINERUNKNOWN REASON.
Patient problems: Insufficient Information
MAUDE report 22800991 ↗InjuryJun 2, 2025Unstable; Adverse Event Without Identified Device or Use Problem; Unstable; Adverse Event Without Identified Device or Use Problem
InjuryAug 21, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 3, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY - REMOVED HEADBALL & PROXIMAL BODY & REPLACED WITH MEW BODY & HEADBALL AFTER WASHOUT.
Patient problems: Insufficient Information
MAUDE report 18441363 ↗InjuryDec 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryMay 10, 2022Appropriate Device Problem Term/Code Not Available
REVSISON SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 14346374 ↗InjuryAug 25, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT HAD A STRYKER DUAL MOBILITY ACETABULAR CUP IN AND ON A EXPERT STEM. SURGEON WENT IN AND REPLACED THE PROXIMAL BODY AND THE CERAMIC HEAD BECAUSE THE PATIENT WAS NOT STABLE.
Patient problems: Insufficient Information
MAUDE report 12367348 ↗InjuryJan 11, 2018Insufficient Device Problem Information
REVISION SURGERY - DUE TO THE PATIENT COMPLAINING OF PAIN. THE SURGEON WENT IN AND REMOVED THE OLD CABLES AND PUT IN NEW ONES TO GET PROXIMAL FIXATION. HE SWAPPED OUT PROXIMAL BODY AND HEAD.
Patient problems: Pain
MAUDE report 7183472 ↗InjuryOct 27, 2017Device Dislodged or Dislocated
REVISION SURGERY - THE PATIENT INITIALLY HAD A SPIRAL FRACTURE AND THE SURGEON HAD PUT IN A STEM AND A SIZE 75 MM PROXIMAL BODY TO ANTICIPATE SUBSIDENCE. THE PROSTHESES DID SUBSIDE AS ANTICIPATED AND SURGEON, DUE TO THE NATURE OF THE FRACTURE, EXTRACTED THE PROXIMAL BODY AND REPLACED WITH A TALLER 85MM PROXIMAL BODY AND WAS PLEASED WITH THE END RESULTS.
Patient problems: Bone Fracture(s); No Code Available
MAUDE report 6985187 ↗
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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