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Dynasty DSPCGD52Recalls & reported problems

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

Adverse event reports
4
Deaths reported
0
Injuries reported
4
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI M684DSPCGD521), received between Feb 26, 2020 and Apr 27, 2022 — classified as 4 injuries.

The most frequently reported specific device problem is “Loss of Osseointegration” (3 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

  • Loss of Osseointegration3
  • Device Dislodged or Dislocated1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
  • No Information1
  • Pain1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 27, 2022Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY, ON TUESDAY, (B)(6) DR (B)(6) REVISED AN ACETABULAR COMPONENT FROM A PREVIOUS SUPERPATH HIP, DYNASTY PC SHELL. PT HAD PRIMARY HIP ON (B)(6) 2020, AND LATER EXPERIENCED GROIN PAIN. DR REVIEWED, ALSO HAD PT RECEIVE A SECOND OPINION. NOT OBVIOUS THAT ANYTHING WRONG BUT WAS THOUGHT MAYBE CUP HAD MOVED. WHEN WE REVISED THEIR WAS SOME MICRO MOTION AND NOT OBVIOUS SIGNS OF BONE INGROWTH. WAS REVISED TO A DIFFERENT COMPANIES CUP. (B)(4).

    Patient problems: Pain

    MAUDE report 14218913 ↗
  • InjuryAug 24, 2021Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY, PATIENT UNDERWENT THR ON (B)(6) 2020, LEFT HIP REVISED ON (B)(6) 2021 DUE TO CUP MOVING. BIOLOX HEAD REVISED WITH A DIFFERENT SIZE, DYNASTY SHELL AND LINER REVISED WITH ANOTHER MANUFACTURER'S MULTI HOLE COMPONENTS. ADDITIONAL HISTORY: THIS IS THE SAME PATIENT AND SAME HIP THAT EXPERIENCED THE ISSUE WHERE THE STEM SAT HIGHER THAN THE BROACH, (B)(4). (B)(6).

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 12360045 ↗
  • InjuryMar 30, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

    ALLEGEDLY, CUP, LINER, SCREW, HEAD EXTRACTED IN FAVOR OF A STRYKER REVISION CUP/CONSTRAINED LINER AND A MP 22 MM HEAD. ADDITIONAL INFORMATION WAS RECEIVED ON 03/17/2021 FROM DISTRIBUTOR: INCIDENT FORM CONTAINING SUBSTANTIAL INFORMATION, ALSO ON THIS DAY, REASON FOR REVISION. ALLEGEDLY, THE PATIENT HAD DISLOCATED SEVERAL TIMES.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 11589405 ↗
  • InjuryFeb 26, 2020Loss of Osseointegration; Loss of Osseointegration

    ALLEGEDLY, PATIENT WAS REVISED DUE TO CORROSION AT THE COCR MODULAR NECK AND TITANIUM STEM, ELEVATED COBALT IONS LEVELS AND LOOSENING OF THE ACETABULAR COMPONENT.

    Patient problems: No Information

    MAUDE report 9758308 ↗

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.