Dynasty DLDMGC38Recalls & reported problems
Microport Orthopedics Inc. · Dynasty® Dual Mobility Liner Group C 38mm · 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 00192629205536), received between Dec 29, 2021 and Dec 29, 2021 — 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
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 29, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, ITEM IMPLANTED ON (B)(6) 2021 WITHOUT INCIDENT, PATIENT PRESENTED AT EMERGENCY ROOM ON (B)(6) 2021 WITH DISLOCATION OF HEAD/LINER CONSTRUCT FORM SHELL/LINER. CLOSED REDUCTION WAS ATTEMPTED AND UNSUCCESSFUL. PATIENT WAS REFERRED TO (B)(6). REVISING SURGEON DECIDED REMOVAL OF ALL IMPLANTS WAS IN BEST INTEREST OF PATIENT. COMPONENTS SUCCESSFULLY EXPLANTED ON (B)(6) 2021. A SALES REPRESENTATIVE WAS PRESENT AT THE PROCESS. PATIENT SUFFERING FROM DEMENTIA AND NON-AMBULATORY.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 13111951 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.