Skip to content

CONSERVE® 38AM3604Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® A-CLASS® BFH® HEAD SHORT NECK 36MM · 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 M68438AM36041), received between Jan 6, 2020 and Oct 13, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

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 Information2
  • Corroded1

Patient problems

  • Metal Related Pathology1
  • No Information1

Recent adverse event reports

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

  • InjuryOct 13, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, PATIENT WAS REVISED DUE TO METAL ON METAL COMPLICATIONS. IMPLANT WAS REMOVED. ADDITIONAL INFORMATION RECEIVED ON 09/23/2020 FROM (B)(6): ADDING PRODUCT INFORMATION AND UPDATING IMPLANT DATE. ADDITIONAL INFORMATION RECEIVED ON 09/25/2020 FROM (B)(6): CONFIRMATION OF THE PRODUCT NUMBER OF THE SHELL.

    Patient problems: Metal Related Pathology

    MAUDE report 10673315 ↗
  • InjuryJan 6, 2020Corroded; Insufficient Device Problem Information; Corroded; Insufficient Device Problem Information

    ALLEGEDLY PATIENT WAS REVISED DUE TO UNKNOWN REASONS. LEFT HIP.

    Patient problems: No Information

    MAUDE report 9554963 ↗

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.