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NA 02.110.300Recalls & reported problems

Synthes GmbH · 1.8MM KIRSCHNER WIRE WITH TROCAR POINT 150MM · Class 2 · Implant

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 20886982030617), received between Feb 20, 2019 and Feb 20, 2019 — classified as 1 malfunction.

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

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionFeb 20, 2019Break; Break

    CONCOMITANT DEVICE REPORTED: UNK - POWER WIRE DRIVER (PART# UNKNOWN, LOT# UNKNOWN, QUANTITY# 1).

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8353667 ↗

Other PIN, FIXATION, SMOOTH devices

All PIN, FIXATION, SMOOTH devices →

Sources and updates

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