CONQUEST FN 75807090Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556530245), received between Feb 19, 2020 and Jun 8, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (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

Recent adverse event reports

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

• InjuryJun 8, 2022Premature Separation; Premature Separation

  IT WAS REPORTED THAT, AFTER AN INTERNAL FIXATION WAS PERFORMED ON AN UNSPECIFIED DATE, THE PATIENT EXPERIENCED A NONUNION FRACTURE AND THE TOP SCREW ON A CONQUEST FN LCK PL 1H L 60MM WAS NOTICED TO BE BACKING OUT. IT IS UNKNOWN HOW THIS ADVERSE EVENT WAS SOLVED. CURRENT HEALTH STATUS OF PATIENT IS UNKNOWN.

  Patient problems: Failure of Implant; Inadequate Osseointegration

  MAUDE report 14637514 ↗
• InjuryFeb 19, 2020Break; Break

  IT WAS REPORTED THAT REVISION WAS PERFORMED DUE TO CONQUEST-FRACTURE COLLAPSED (SO IT WAS CONVERTED TO TOTAL HIP). THE PATIENT DID NOT FALL BUT WAS COMPLAINING OF PAIN. THEY FOUND IN X-RAYS BROKEN SCREWS.

  Patient problems: Injury

  MAUDE report 9727369 ↗