CONQUEST FN 75808095Recalls & reported problems
Smith & Nephew, Inc. · CONQUEST FN 8.5MM X 95MM PROXIMAL LOCKING SCREW STAINLESS STEEL 20MM THREAD · Class 2
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 00885556530368), 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 9727294 ↗
Other DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT devices
- NA 282.238Synthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- 13 X 90mm LAG FASTENER 324-13090Osteocentric Technologies, Inc. · Device, Fixation, Proximal Femoral, Implant1 report
- DHS 281.031Synthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 281.520SSynthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 280.285SSynthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 281.504Synthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- CONQUEST FN 71179203Smith & Nephew, Inc. · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- PERCUTANEOUS COMPRESSION PLATE (PC.C.P) 1Orthofix Srl · Device, Fixation, Proximal Femoral, Implant1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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