Skip to content

CONQUEST FN 71179203Recalls & reported problems

Smith & Nephew, Inc. · CONQUEST FN PROXIMAL LOCKING SCREW DRILL GUIDE · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556533086), received between Feb 28, 2022 and Feb 28, 2022 — classified as 1 malfunction.

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

Most reported problems

Device problems

  • Break1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 28, 2022Break; Break

    IT WAS REPORTED THAT, DURING USE, THE THREADS OF THE CONQUEST FN PROX LCK SCR DRILL GUIDE STRIPPED AND BROKE OFF. A BACK-UP DEVICE WAS AVAILABLE. IT IS UNKNOWN IF THERE WAS A DELAY DUE TO THIS EVENT. NO PATIENT COMPLICATIONS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13625971 ↗

Other DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT devices

All DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page