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CONSERVE® 38AC3800Recalls & reported problems

Microport Orthopedics Inc. · CONSERVE® TOTAL A-CLASS® 38MM 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 M68438AC38001), received between Apr 26, 2021 and Apr 26, 2021 — 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

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • InjuryApr 26, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, PATIENT WAS REVISED DUE TO UNKNOWN REASONS. COMPONENTS NOT REVISED: DYNASTY® A-CLASS® 38MM 15DG GROUP E CROSSLINKED POLY LINER PRODUCT ID: DLXPLE38 LOT: 0501142452. DYNASTY® BF SHELL 54MM GROUP E PRODUCT ID: DSBFGE54 LOT: 1201210358. PROFEMUR® Z FEMORAL STEM S 2 1/3 TP COATED CEMENT LESS PRODUCT ID: PHA00262 LOT: 0901201577. CANCELLOUS SELF-TAPPING 6.5MM BONE SCREW 2.5CM LENGTH PRODUCT ID: 18080302 LOT: 0111294020.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11727398 ↗

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.