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LARGE CANNULATED SCREWS 71119110Recalls & reported problems

Smith & Nephew, Inc. · SOLID CAPTIVE HEX DRIVER REVERSE TWIST 4.7MM HEX · Class 1

All models of LARGE CANNULATED SCREWS (21)

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 03596010428103), received between May 21, 2021 and May 21, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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

  • Physical Resistance/Sticking1

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.

  • MalfunctionMay 21, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

    IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGERY, THE PHYSICIAN WAS HAVING ISSUES REMOVING SCREWS FROM THE REV TWIST HEX 4.7MM SOLID. THE SAME DEVICE STRIPPED A CANNULATED SCREW. IS IT UNKNOWN HOW THE PROCEDURE WAS FINISHED, WHEN THE EVENT OCCURRED AND IF THERE WAS A DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11861486 ↗

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Sources and updates

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