CONSERVE® 38AM3600Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® A-CLASS® BFH® HEAD MEDIUM NECK 36MM · Class 3 · 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 M68438AM36001), received between Mar 24, 2020 and Jan 26, 2021 — classified as 2 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.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
- Material Disintegration1
Patient problems
- Metal Related Pathology1
- Reaction1
- Unequal Limb Length1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 26, 2021Material Disintegration; Device Dislodged or Dislocated; Material Disintegration; Device Dislodged or Dislocated
ALLEGEDLY, THE PATIENT UNDERWENT A REVISION SURGERY DUE TO DISLOCATION, METAL DEBRIS WITH PSEUDO-TUMOR FORMATION AND LEG LENGTH DISCREPANCY. COMPONENT NOT REVISED: DSPCGC50 DYNASTY® PC SHELL 50MM, GROUP C, LOT: 129999843.
Patient problems: Metal Related Pathology; Unequal Limb Length
MAUDE report 11230126 ↗InjuryMar 24, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO METAL ON METAL COMPLICATIONS.
Patient problems: Reaction
MAUDE report 9875294 ↗
Other Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component) devices
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- RingLoc® Hip System 103531Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)1 recall0 reports
- BIOLOX DELTA 1365-28-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)43 reports
- ASPHERE 1365-52-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)39 reports
- ASPHERE 1365-05-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)29 reports
- ASPHERE 1365-06-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)29 reports
- Taperloc Complete Micro Primary Femoral 51-107130Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)23 reports
- Taperloc Complete Micro Primary Femoral 51-107120Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)19 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.