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HEX-FIX 122700Recalls & reported problems

Smith & Nephew, Inc. · TITANIUM HALF PIN 4.0MM X 20MM · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010069344), received between Jun 27, 2019 and Jun 27, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (2 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.

Most reported problems

Device problems

  • Break2

Patient problems

  • Injury2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 27, 2019Break; Break

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO THE BREAKAGE OF HALF PINS.

    Patient problems: Injury

    MAUDE report 8739217 ↗
  • InjuryJun 27, 2019Break; Break

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO THE BREAKAGE OF HALF PINS.

    Patient problems: Injury

    MAUDE report 8739216 ↗

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Sources and updates

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