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SMALL CANNULATED SCREWS 71103226SRecalls & reported problems

Smith & Nephew, Inc. · 3.0MM CANNULATED SCREW 26MM STERILE · Class 2 · Implant

All models of SMALL CANNULATED SCREWS (18)

Data updated Oct 18, 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 03596010623904), received between Jul 13, 2023 and Jul 13, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Device Embedded In Tissue or Plaque1

Recent adverse event reports

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

  • InjuryJul 13, 2023Fracture; Fracture

    IT WAS REPORTED THAT DURING A MEDIAL EPICONDYLE ON A DISTAL HUMERUS, WHEN INSERTING THE 3.0MM CANNULATED SCREW 26MM, IT TOOK AN X-RAY WHEN THE SCREW WAS 2/3 OF THE WAY IN AND NOTICED THE SELF DRILLING TIP BROKE OFF. THE TIP WAS IN THE PATIENT. TIP OF SCREW WAS LEFT INSIDE PATIENT'S BONE. THE PROCEDURE WAS RESUMED, AFTER A NON-SIGNIFICANT DELAY, WITH A S+N BACK-UP DEVICE. NO OTHER COMPLICATIONS WERE REPORTED.

    Patient problems: Device Embedded In Tissue or Plaque

    MAUDE report 17321231 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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