Conserve 38AM5200Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® A-Class® BFH® Femoral Head Medium Neck 52mm · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00192629060821), received between Nov 6, 2020 and Oct 23, 2023 — classified as 2 injuries, 1 malfunction.
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
- Appropriate Device Problem Term/Code Not Available1
- Corroded1
- Fracture1
Patient problems
- Metal Related Pathology2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 23, 2023Corroded; Corroded
ALLEGEDLY, COCR CORROSION CLAIM (10+). LEFT SIDE.
Patient problems: Insufficient Information
MAUDE report 17987564 ↗InjuryJan 6, 2022Appropriate Device Problem Term/Code Not Available
ALLEGEDLY THE PATIENT WAS REVISED DUE TO MOM COMPLICATIONS - LEFT SIDE.
Patient problems: Metal Related Pathology
MAUDE report 13177611 ↗InjuryNov 6, 2020Fracture
ALLEGEDLY, ON (B)(6) 2020 THE FEMORAL NECK OF THE DEVICE FAILED FRACTURING INTO TWO PIECES, ON THAT SAME DATE THE DEVICE WAS SURGICALLY REMOVED. DURING THE REVISION PROCEDURE THE DOCTOR OBSERVED METALLOSIS DEEP IN THE HIP. (RIGHT HIP).
Patient problems: Metal Related Pathology
MAUDE report 10800693 ↗
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- "UNITED" USTAR II Knee System 2515-3115United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- STAGEONE 431207Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3111United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- ACTIS 101011050Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal73 reports
- UHR UH1-46-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
- UHR UH1-45-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.