Dynasty DBFRGC50Recalls & reported problems
Microport Orthopedics Inc. · DYNASTY® BF SHELL REVISION 50MM GROUP C · Class 2 · Implant
All models of Dynasty (44)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684DBFRGC501), received between Dec 29, 2021 and Dec 29, 2021 — classified as 1 injury.
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 18, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 29, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, ITEM IMPLANTED ON (B)(6) 2021 WITHOUT INCIDENT, PATIENT PRESENTED AT EMERGENCY ROOM ON (B)(6) 2021 WITH DISLOCATION OF HEAD/LINER CONSTRUCT FORM SHELL/LINER. CLOSED REDUCTION WAS ATTEMPTED AND UNSUCCESSFUL. PATIENT WAS REFERRED TO TULSA. REVISING SURGEON DECIDED REMOVAL OF ALL IMPLANTS WAS IN BEST INTEREST OF PATIENT. COMPONENTS SUCCESSFULLY EXPLANTED ON (B)(6) 2021. A SALES REPRESENTATIVE WAS PRESENT AT THE PROCESS. PATIENT SUFFERING FROM DEMENTIA AND NON-AMBULATORY.
Patient problems: Failure of Implant
MAUDE report 13109224 ↗
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- EXETER 0580-1-351Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous29 reports
- INSTRUMENT 2101-0200Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous27 reports
- REFLECTION 71330001Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous20 reports
- Accolade 6720-0330Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous18 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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