CONSERVE® 38015435Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® BFH® HEAD 54MM LONG NECK · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684380154351), received between Jun 14, 2022 and Aug 3, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Noise, Audible1
Patient problems
- Insufficient Information1
- Metal Related Pathology1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 3, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT WAS REVISED DUE TO DISLOCATION/SUBLUXATION. REVISION NJR NUMBER: (B)(4). SIDE:R. PRIMARY ASA: P1 - FIT AND HEALTHY. COMPONENTS NOT REVISED: 1-PARTID: PHA05514, PROFEMUR® L HIP STEM SIZE 7 HA COATED, LOT: V04150751, QTY:1. 2-PARTID: PHA01202, PROFEMUR® NECK NEUTRAL SHORT, LOT: V11287405, QTY:1.
Patient problems: Insufficient Information
MAUDE report 15156153 ↗InjuryJun 14, 2022Noise, Audible; Noise, Audible
ALLEGEDLY THE PATIENT REPORT "CLICKING AND POPPING" SOUNDS FROM HIS RIGHT HIP, THE DR NOTED AUDIBLE AND PALPABLE POPPING OF THE RIGHT HIP WITH FLEXION, AND THE RADIOGRAPHIC IMAGES REVEALED THAT THE WRIGHT MEDICAL CONSERVE HIP FAILED AND THE PATIENT WAS SUFFERING FROM ELEVATED COBALT CHROME LEVELS.
Patient problems: Metal Related Pathology
MAUDE report 14690688 ↗
Other Prosthesis, Hip, Hemi-, Femoral, Metal devices
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- "UNITED" USTAR II Knee System 2515-3213United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3115United 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 2515-3111United 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.