Skip to content

CONSERVE® 38AM4200Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® A-CLASS® BFH® HEAD MEDIUM NECK 42MM · 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 M68438AM42001), received between Jun 18, 2019 and Jun 18, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryJun 18, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    ALLEGEDLY, PATIENT REVISED DUE TO THE HEAD SEPARATING FROM THE SHAFT. (PATIENT WAS NOT VERY CLEAR ON THIS).

    Patient problems: No Information

    MAUDE report 8708380 ↗

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.