ANTHOLOGY 71357112Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010559678), received between May 5, 2023 and May 10, 2023 — classified as 2 injuries.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 10, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED, THAT DURING A RIGHT THA REVISION SURGERY PERFORMED ON THE (B)(6) 2022, THE GREATER TROCHES FRACTURE WHILE TRYING TO EXPOSE THE FEMORAL COMPONENT WHICH WAS TREATED WITH BONE GRAFT. ADDITIONALLY, DURING THE PROCEDURE, THERE WAS CONCERN OF BLOOD LOSS FROM THE ACETABULAR COMPONENT, THEREFORE TWO UNITS OF PACKED RED BLOOD CELLS WERE PROVIDED. THE PATIENT WAS STABLE AT THE END OF THE PROCEDURE.

  Patient problems: Bone Fracture(s); Hemorrhage/Blood Loss/Bleeding

  MAUDE report 16903520 ↗
• InjuryMay 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT, AFTER A RIGHT THA SURGERY WAS PERFORMED ON THE 28-AUG-2008 DUE TO OSTEOARTHRITIS, THE PATIENT EXPERIENCED IN 2017, A PROXIMAL FEMUR FRACTURE WHICH WAS TREATED CONSERVATIVELY. NO FURTHER INFORMATION AVAILABLE.

  Patient problems: Bone Fracture(s)

  MAUDE report 16876256 ↗