ANTHOLOGY 71357006Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010559494), received between May 22, 2019 and Mar 9, 2021 — classified as 3 injuries.

The most frequently reported specific device problem is “Fracture” (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. 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO A PROXIMAL FEMUR PERIPROSTHETIC FRACTURE. THE ENTIRE FEMORAL COMPONENT WAS REVISED. THE OUTCOME IS RESOLVED.

  Patient problems: Bone Fracture(s)

  MAUDE report 11449618 ↗
• InjuryOct 29, 2019Fracture; Fracture

  IT WAS REPORTED THAT THE PATIENT SUFFERED A FEMORAL FRACTURE DURING AN OPERATION. IT IS UNKNOWN IF THERE WAS A DELAY OR IF A BACKUP DEVICE WAS AVAILABLE.

  Patient problems: Injury

  MAUDE report 9253283 ↗
• InjuryMay 22, 2019Loose or Intermittent Connection; Loose or Intermittent Connection

  IT WAS REPORTED THAT PATIENT HAD A TOTAL HIP ARTHROPLASTY ON (B)(6) 2013 AND 2 MONTHS LATER, THE STEM WAS CONFIRMED WHICH HAD SUBSIDED.

  Patient problems: Injury

  MAUDE report 8634428 ↗