CONSERVE® 38014600Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® BFH® HEAD 46MM MEDIUM NECK · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M684380146001), received between Jan 21, 2021 and Mar 20, 2024 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Appropriate Device Problem Term/Code Not Available1
- Device Dislodged or Dislocated1
Patient problems
- Metal Related Pathology3
- Loss of Range of Motion1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 20, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, LOOSENING ? STEM/LYSIS ? STEM/PERI-PROSTHETIC FRACTURE ? STEM/DISLOCATION/SUBLUXATION/ADVERSE SOFT TISSUE REACTION TO PARTICULATE. DEBRIS. SIDE: R. REVISION NJR: (B)(4). GENDER: M. EXPLANTED: FEMORAL STEM, ACETABULAR CUP (NOT MPO COMPONENTS).
Patient problems: Metal Related Pathology
MAUDE report 18940274 ↗InjurySep 6, 2022Appropriate Device Problem Term/Code Not Available
ALLEGEDLY, PATIENT WAS REVISED DUE TO ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS REVISION NJR NUMBER: (B)(4). SIDE:R. PRIMARY ASA: P1 - FIT AND HEALTHY. PRODUCTS NOT REVISED: 1-PRODUCT ID: PHA00240, PROFEMUR® Z FEMORAL STEM SIZE 5 CEMENTLESS, LOT NUMBER: NI, QTY: 1. 2-PRODUCT ID: PHA01202, PROFEMUR® NECK NEUTRAL SHORT, LOT NUMBER: NI, QTY: 1.
Patient problems: Metal Related Pathology
MAUDE report 15365902 ↗InjuryJan 21, 2021Adverse Event Without Identified Device or Use Problem
ALLEGEDLY, PATIENT UNDERWENT A LEFT TOTAL HIP REPLACEMENT AND RECEIVED A MOM HIP SYSTEM IMPLANTS. PATIENT SUFFERED PAIN, LACK OF MOBILITY AND HIGH LEVELS OF TOXIC METAL LEVELS.
Patient problems: Loss of Range of Motion; Metal Related Pathology; Pain
MAUDE report 11208127 ↗
Other Prosthesis, Hip, Hemi-, Femoral, Metal devices
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- "UNITED" USTAR II Knee System 2515-3213United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- "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.