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