CONSERVE® 38014200Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® BFH® HEAD 42MM MEDIUM NECK · Class 2 · 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 M684380142001), received between Feb 2, 2021 and Feb 21, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Corroded” (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.
Reports received per month
Most reported problems
Device problems
- Corroded1
- Insufficient Device Problem Information1
- Material Disintegration1
Patient problems
- Metal Related Pathology2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 21, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS, SIDE: L, REVISION NJR: 1387922, GENDER: F, EXPLANTED: ACETABULAR CUP (NOT AN MPO COMPONENT).
Patient problems: Metal Related Pathology
MAUDE report 18750905 ↗InjuryFeb 2, 2021Corroded; Material Disintegration; Corroded; Material Disintegration
ALLEGEDLY, THE PATIENT WAS REVISED DUE TO METAL DEBRIS, CORROSION AND RESULTANT METAL IONS DUE TO THE METAL-ON-METAL DESIGN BETWEEN THE ARTICULATING SURFACES.
Patient problems: Metal Related Pathology
MAUDE report 11268519 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.