Skip to content

CONSERVE® 38015035Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® BFH® HEAD 50MM LONG NECK · Class 3 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684380150351), received between Aug 4, 2023 and Aug 4, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Metal Related Pathology1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 4, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, ON (B)(6) 2023 WE RECEIVE A COMPLAINT NOTIFICATION FROM AOU PISANA ON THR WITH CONSERVE. FIRST SURGERY DONE IN 2006 IN A DIFFERENT HOSPITAL AND FOR THIS REASON IT'S IMPOSSIBLE TO RETRIEVE MORE INFO AND DETAILS. IN THE EXAMINATION THE PATIENT WAS DIAGNOSED WITH A METALLOSIS WHICH MADE NECESSARY TO REMOVE CUP, HEAD, STEM AND MODULAR NECK. UNFORTUNATELY, NO INFO AVAILABLE ON STEM AND NECK.

    Patient problems: Metal Related Pathology

    MAUDE report 17461372 ↗

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

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

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