CONSERVE® 38031042Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® FEMORAL RESURFACING HEAD 42MM · 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 M684380310421), received between Feb 3, 2021 and Apr 1, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (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.
Reports received per month
Most reported problems
Device problems
- Loss of Osseointegration2
Patient problems
- Insufficient Information1
- Metal Related Pathology1
- Osteolysis1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 1, 2024Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, PATIENT WAS REVISED DUE TO LOOSENING - STEM. REVISION NJR NUMBER: 5181801. SIDE:L. PRIMARY ASA: P1 - FIT AND HEALTHY.
Patient problems: Insufficient Information
MAUDE report 19013107 ↗InjuryFeb 3, 2021Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, PATIENT WAS REVISED DUE TO ASEPTIC LOOSENING SOCKET; ASEPTIC LOOSENING STEM; LYSIS SOCKET; LYSIS STEM; PAIN; ADVERSE SOFT TISSUE REACTION TO PARTICLE DEBRIS REVISION NJR NUMBER: (B)(4). SIDE:R. PRIMARY ASA: P3 - INCAPACITATING SYSTEMIC DISEASE. MHRA REFERENCE NO: (B)(4).
Patient problems: Metal Related Pathology; Osteolysis; Pain
MAUDE report 11273433 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.