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CONSERVE® 38AC5000Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® TOTAL A-CLASS® 50MM FEMORAL HEAD · 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 M68438AC50001), received between May 20, 2020 and May 20, 2020 — 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

  • Reaction1

Recent adverse event reports

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

  • InjuryMay 20, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, METAL ON METAL, CUP MAY BE LOOSE. CUP, HEAD, NECK AND THE NECK SLEEVE WERE CAME OUT. ADDITIONAL INFORMATION: RIGHT HIP.

    Patient problems: Reaction

    MAUDE report 10075446 ↗

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.