Skip to content

Dynasty DSBFGB48Recalls & reported problems

Microport Orthopedics Inc. · DYNASTY® BF SHELL 48MM GROUP B · Class 3 · Implant

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 M684DSBFGB481), received between May 20, 2019 and May 20, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 20, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY THE PATIENT UNDERWENT THR ON (B)(6) 2019, REVISED ON (B)(6) 2019 DUE TO PERI-PROSTHETIC FRACTURE. REVISING SURGEON BELIEVES FRACTURE WAS CAUSED INTRA-OPERATIVELY. NO X-RAYS AVAILABLE.

    Patient problems: Bone Fracture(s)

    MAUDE report 8623392 ↗

Other Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) devices

All Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.