Skip to content

Dynasty DBFPGF56Recalls & reported problems

Microport Orthopedics Inc. · DYNASTY® BF SHELL PRIMARY 56MM GROUP F · Class 2 · 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 M684DBFPGF561), received between Mar 30, 2022 and Mar 30, 2022 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1
  • Loss of Osseointegration1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryMar 30, 2022Loss of Osseointegration; Device Dislodged or Dislocated; Loss of Osseointegration; Device Dislodged or Dislocated

    PT. DISLOCATED. REVISED CUP (REPOSITIONED). PRODUCT NO REVISED: PRODUCT ID: PHAPE242 PROFEMUR Z 6 LONG VARUS STEM, LOT: 1906933, QTY: 1.

    Patient problems: Insufficient Information

    MAUDE report 13955720 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices →

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