CONQUEST FN 71179215Recalls & reported problems
Smith & Nephew, Inc. · CONQUEST FN SCREWDRIVER · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00885556683613), received between May 22, 2018 and Feb 18, 2025 — classified as 1 injury, 5 malfunctions.
The most frequently reported specific device problem is “Break” (5 reports).
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.
Reports received per month
Most reported problems
Device problems
- Break5
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Consequences Or Impact To Patient2
- No Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2025Fracture; Fracture
IT WAS REPORTED THAT, DURING AN INTERNAL FIXATION SURGERY, THE OUTDENT OF THREE (3) CONQUEST FN SCREWDRIVERS SNAPPED OFF, SO SCREWDRIVERS WOULD NOT ENGAGE SCREW. THE PROCEDURE WAS RESUMED, AFTER A NON-SIGNIFICANT DELAY, WITH A CHANGE IN SURGICAL TECHNIQUE. NO INJURY WAS REPORTED AS A CONSEQUENCE OF THIS ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21396581 ↗MalfunctionFeb 23, 2022Break; Break
IT WAS REPORTED THAT TWO (2) CONQUEST FN SCREWDRIVER ARE BROKEN. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13588142 ↗MalfunctionSep 25, 2020Break; Break
IT WAS REPORTED THAT DURING SURGERY OUTSIDE OF THE PATIENT, THE SCREWDRIVER AND THE EXTENSION ROD BOTH GOT BROKEN, AS WELL AS A MISSING PIECE THAT HOLDS THE SCREW IN BOTH POSITIONS. THERE WAS NO DELAY NOR INJURY REPORTED. A S&N BACKUP DEVICE WAS AVAILABLE TO FINISHED THE SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 10584928 ↗MalfunctionSep 25, 2020Break; Break
IT WAS REPORTED THAT DURING SURGERY OUTSIDE OF THE PATIENT, THE SCREWDRIVER AND THE EXTENSION ROD BOTH GOT BROKEN, AS WELL AS A MISSING PIECE THAT HOLDS THE SCREW IN BOTH POSITIONS. THERE WAS NO DELAY NOR INJURY REPORTED. A S&N BACKUP DEVICE WAS AVAILABLE TO FINISHED THE SURGERY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10584926 ↗MalfunctionSep 27, 2018Break; Break
IT WAS REPORTED THAT THE CLIPS THAT HOLD SCREW ON BROKE.
Patient problems: No Information
MAUDE report 7914049 ↗InjuryMay 22, 2018Break; Break
IT WAS REPORTED THAT TOWARDS THE END OF THE SURGERY IT LOOKED LIKE THE DEVICES NEEDED MORE FORCE AND THE SURGEON KEPT TURNING THE DRIVERS UNTIL IT SNAPPED OFF. FOUR DRIVERS WERE BROKEN IN THE SAME WAY. THERE WAS MINIMAL DELAY TO REMOVE SCREW DRIVER FRAGMENTS FROM PATIENT. DOCTOR VERIFIED WITH X RAYS THAT THE DEVICES WERE REMOVED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7531978 ↗
Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices
- PRECICE® Plating System LP4.5-DLF31Nuvasive Specialized Orthopedics, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component3 recalls0 reports
- R3 71364451Smith & Nephew, Inc. · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT145 reports
- DFS HA BONE SCREWS HAA60-11030Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAB60-12040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-18040Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15060Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
- DFS HA BONE SCREWS HAA60-15020Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT2 recalls0 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page