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LARGE CANNULATED SCREWS 71177133Recalls & reported problems

Smith & Nephew, Inc. · 4.7MM BALL HEXDRIVER SHAFT W/QUICK CONNECT · Class 1

All models of LARGE CANNULATED SCREWS (21)

Data updated Oct 18, 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 03596010601513), received between May 13, 2021 and May 13, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (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 18, 2026.

Most reported problems

Device problems

  • Mechanical Jam1

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 13, 2021Mechanical Jam; Mechanical Jam

    IT WAS REPORTED THAT, AFTER A TRAUMA SURGERY, A 4.7MM BALL HEXDRIVER WAS STUCK INSIDE TEARDROP HANDLE WITH LARGE AO. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT DELAY USING A SMITH AND NEPHEW BACK UP DEVICE. PATIENT WAS NOT HARMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11822115 ↗

Other SCREWDRIVER devices

All SCREWDRIVER devices →

Sources and updates

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