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CONSERVE® 38AM5035Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® A-CLASS® BFH® HEAD LONG NECK 50MM · Class 3 · 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 M68438AM50351), received between Jan 29, 2020 and Jul 13, 2020 — classified as 2 injuries.

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

  • Appropriate Device Problem Term/Code Not Available2

Patient problems

  • Reaction2
  • Osteolysis1
  • Pain1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 13, 2020Appropriate Device Problem Term/Code Not Available

    ALLEGEDLY, PATIENT WAS REVISED DUE TO METAL ON METAL COMPLICATIONS OF HIS LEFT HIP.

    Patient problems: Osteolysis; Pain; Reaction

    MAUDE report 10268140 ↗
  • InjuryJan 29, 2020Appropriate Device Problem Term/Code Not Available

    ALLEGEDLY, HEAD AND NECK WERE PULLED AND REPLACED WITH THE SAME NECK AND A 28 CERAMIC HEAD/LONG SLEEVE. METAL ON METAL WAS THE REASON FOR REVISION. CONSERVE CUP ALSO REVISED.

    Patient problems: Reaction

    MAUDE report 9644967 ↗

Other Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) devices

All Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.