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CONQUEST FN 75807003LRecalls & reported problems

Smith & Nephew, Inc. · CONQUEST FN LOCKING PLATE 3 HOLE LEFT 127MM · Class 2 · Implant

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556530207), received between Feb 19, 2020 and Feb 19, 2020 — classified as 1 injury.

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

  • Injury1

Recent adverse event reports

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

  • 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 9727250 ↗

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices

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Sources and updates

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