Dynasty DSBFGC50Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® BF SHELL 50MM GROUP C · Class 3 · Implant
All models of Dynasty (44)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 M684DSBFGC501), received between Oct 16, 2019 and Jul 15, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
Patient problems
- Hip Fracture1
- Unspecified Tissue Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT REVISED DUE TO COPIOUS AMOUNT OF BLACK DISCOLORED TISSUE, BLACK DISCOLORATION OF THE JOINT CAPSULE CONSISTENT WITH METALLOSIS AND DISLOCATION. (LEFT HIP)
Patient problems: Unspecified Tissue Injury
MAUDE report 12178689 ↗InjuryOct 16, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PERIPROSTHETIC FRACTURE OF THE ACETABULAR COMPONENT PATIENT WAS SEEN IN CLINIC POST SX BETWEEN JUL 2015-JAN 2013. IMPROVEMENTS WERE SLOW. PATIENT WAS NOT FULLY WEIGHT BEANING. PATIENT ENDED UP HAVING A FAILED ACETABULAR ON (B)(6) 2013, THE PATIENT UNDERWENT A REVISION WITH CAGE RECONSTRUCTION.
Patient problems: Hip Fracture
MAUDE report 9199995 ↗
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 1365-06-100Depuy (Ireland) · Prosthesis, hip, semi-constrained (metal uncemented acetabular component)29 reports
- ASPHERE 1365-05-100Depuy (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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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