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Dynasty DBFPGD52Recalls & reported problems

Microport Orthopedics Inc. · DYNASTY® BF SHELL PRIMARY 52MM GROUP D · Class 2 · Implant

Adverse event reports
5
Deaths reported
0
Injuries reported
5
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI M684DBFPGD521), received between Jun 3, 2020 and Sep 4, 2023 — classified as 5 injuries.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component2
  • Loss of Osseointegration2
  • Adverse Event Without Identified Device or Use Problem1
  • Device Dislodged or Dislocated1
  • Failure to Osseointegrate1
  • Naturally Worn1

Patient problems

  • No Information2
  • Hypersensitivity/Allergic reaction1
  • Insufficient Information1
  • Pain1
  • Unspecified Infection1

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • InjurySep 4, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    ALLEGEDLY, THE PATIENT WHO UNDERWENT TOTAL HIP REPLACEMENT PERFORMED ELSEWHERE AND HAS DEVELOPED RECURRENT DISLOCATIONS OF THE HIP AND HAS HAD 3 DISLOCATIONS SINCE (B)(6) 2022. SHE HAS FAILED NONOPERATIVE MANAGEMENT CONSISTING OF ACTIVITY MODIFICATION, PHYSICAL THERAPY AND EDUCATION.

    Patient problems: Insufficient Information

    MAUDE report 17676595 ↗
  • InjuryAug 30, 2021Adverse Event Without Identified Device or Use Problem

    ALLEGEDLY, PATIENT HAD AN ALLERGIC REACTION DUE TO IMPLANTATION OF HIP SYSTEM.

    Patient problems: Hypersensitivity/Allergic reaction

    MAUDE report 12389202 ↗
  • InjuryMar 2, 2021Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY, CUP LOOSENED AND CAUSING WEIGHT BEARING PAIN. BLOOD PATHOLOGY INDICATED INFECTION. ALL PROSTHESIS REMOVED (ETO WAS PREFORMED ON FEMORAL STEM) AND ANTIBIOTIC CEMENT SPACER IMPLANTED. PHOTO'S OF X-RAY AND REMOVED IMPLANTS WERE PROVIDED.

    Patient problems: Pain; Unspecified Infection

    MAUDE report 11398240 ↗
  • InjuryJul 29, 2020Failure to Osseointegrate; Loss of Osseointegration; Device Dislodged or Dislocated; Failure to Osseointegrate; Loss of Osseointegration; Device Dislodged or Dislocated

    ALLEGEDLY, RIGHT LEG IS SHORT, CUP IS TOO VERTICAL, PATIENT HAS DISLOCATED 3 TIMES AND THERE IS LUCENCY AROUND THE CUP TO INDICATED THAT IT HAS POOR IN GROWTH. CUP, SCREWS /LINER/HEAD/NECK WERE PULLED. STRYKER CUP WENT IN WITH OUR HEAD AND NECK.

    Patient problems: No Information

    MAUDE report 10341205 ↗
  • InjuryJun 3, 2020Detachment of Device or Device Component; Naturally Worn; Detachment of Device or Device Component; Naturally Worn

    ALLEGEDLY THE SURGEON REPORTED THAT THE INSERT WAS LOOSE AND ROLLED INSIDE THE SHELL. THE CUP, INSERT, HEAD AND NECK WERE REVISED. HEAD WAS ARTICULATING DIRECTLY ON THE SHELL. PRE-OP X-RAY AND COMPONENTS INCLUDED.

    Patient problems: No Information

    MAUDE report 10115138 ↗

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.