Dynasty DSBFGG58Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® BF SHELL 58MM GROUP G · 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 M684DSBFGG581), received between Jan 10, 2020 and Feb 2, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Most reported problems
Device problems
- Device Dislodged or Dislocated2
Patient problems
- Metal Related Pathology1
- No Information1
- Pain1
- Swelling/ Edema1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 2, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, THE PATIENT EXPERIENCED DISLOCATION, LOSS OF MOBILITY, SWELLING, ADVERSE TISSUE REACTION, AND PAIN DUE TO METAL-ON-METAL COMPONENTS.
Patient problems: Metal Related Pathology; Pain; Swelling/ Edema
MAUDE report 16282926 ↗InjuryJan 10, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT WAS REVISED ON DUE TO THE PATIENT DISLOCATING. ALL COMPONENTS REMOVED, REPLACED WITH DIFFERENT MANUFACTURERS SYSTEM, APART FROM THE 36MM MPO FEMORAL HEAD, WHICH WAS REMOVED AND REPLACED WITH A 28MM MPO FEMORAL HEAD. (B)(6).
Patient problems: No Information
MAUDE report 9577049 ↗
Other Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component) devices
- BIOLOX DELTA 1365-32-730Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)93 reports
- 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.