Dynasty DSBFGF56Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI M684DSBFGF561), received between Aug 6, 2019 and Apr 30, 2025 — classified as 5 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

Recent adverse event reports

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

• InjuryApr 30, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, THE PATIENT UNDERWENT L THR ON (B)(6) 2020. REVISED ON (B)(6) 2020 DUE TO METALLOSIS. FEMORAL HEAD REVISED WITH ANOTHER MPO HEAD, SHELL AND LINER REVISED WITH ANOTHER MANUFACTURER'S ACETABULAR COMPONENTS. REF (B)(4). NON-MPO DEVICES: 1. ACETABULAR INSERT REF: (B)(4). 2. ACETABULAR SHELL REF: (B)(4).

  Patient problems: Metal Related Pathology

  MAUDE report 21939892 ↗
• InjurySep 13, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ALLEGEDLY, PATIENT UNDERWENT LEFT THR ON (B)(6) 2017. REVISED ON (B)(6) 2022 DUE TO DISLOCATION. INITIALLY SURGEON REPLACED HEAD, THEN CUP, THEN STEM UNTIL HIP EVENTUALLY BECAME STABLE. ALL COMPONENTS REMOVED AND REPLACED WITH ANOTHER MANUFACTURER'S SYSTEM. AUSTRALIA (B)(4).

  Patient problems: Failure of Implant

  MAUDE report 15414346 ↗
• InjuryAug 19, 2022Corroded

  ALLEGEDLY, THE PATIENT ON (B)(6) 2020 HAD A LEFT REVISION SURGERY DUE TO CORROSION, ON (B)(6) 2020 THE PATIENT WAS REVISED AGAIN DUE TO INFECTION ON THE SIDE LEFT.

  Patient problems: Unspecified Infection

  MAUDE report 15259802 ↗
• InjuryJul 13, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DO TO UNKNOWN REASONS, AFTER A RIGHT TOTAL HIP ARTHROPLASTY.

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

  MAUDE report 12158428 ↗
• InjuryAug 6, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

  ALLEGEDLY THE PATIENT HAS DISLOCATED 3 TIMES, (B)(6) PA. THE ABOVE IMPLANTS WERE REMOVED FROM THE PATIENT AND REPLACED WITH STRYKERS. STRYKERS DUAL MOBILITY WAS USED WITH A 28MM + 7MM HEAD OF OURS.

  Patient problems: No Information

  MAUDE report 8865602 ↗