CONSERVE® 38014000Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® BFH® HEAD 40MM 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 M684380140001), received between Jun 30, 2021 and Feb 28, 2024 — classified as 2 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
Patient problems
- Metal Related Pathology1
- Paralysis1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 28, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS SIDE: R REVISION NJR: (B)(4). GENDER: F EXPLANTED: FEMORAL STEM, ACETABULAR CUP
Patient problems: Metal Related Pathology
MAUDE report 18797066 ↗InjuryJun 30, 2021Adverse Event Without Identified Device or Use Problem
ALLEGEDLY, AFTER A RIGHT HIP ARTHROPLASTY, PATIENT WAS REVISED DUE TO PAIN. REVISION SURGERY WAS PERFORMED IN 2018 IN (B)(6). FAGG - AFMPS REFERENCE NO: (B)(4).
Patient problems: Paralysis
MAUDE report 12094139 ↗
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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.