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Dynasty DBFPGG60Recalls & reported problems

Microport Orthopedics Inc. · DYNASTY® BF SHELL PRIMARY 60MM GROUP G · 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 M684DBFPGG601), received between Mar 24, 2020 and Mar 24, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryMar 24, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY , PATIENT REVISED DUE TO UNKNOWN FAILURE.

    Patient problems: No Information

    MAUDE report 9873821 ↗

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