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CONSERVE® 38AC5400Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® TOTAL A-CLASS® 54MM FEMORAL HEAD · Class 3 · Implant

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M68438AC54001), received between Dec 18, 2019 and Feb 13, 2020 — classified as 1 injury, 1 malfunction.

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

Patient problems

  • Reaction1
  • Unspecified Infection1

Recent adverse event reports

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

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

    METAL ON METAL HEAD, SLEEVE AND NECK WERE REMOVED AND WERE REPLACED WITH OUR 28 L CERAMIC HEAD, LONG STRAIGHT NECK AND STRIKERS DUAL MOBILITY.

    Patient problems: Reaction

    MAUDE report 9705998 ↗
  • InjuryDec 18, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, INFECTED ALL IMPLANTS WILL BE PULLED.

    Patient problems: Unspecified Infection

    MAUDE report 9490866 ↗

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.