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3M™ 2346NRecalls & reported problems

3m Company · 3M™ Defibrulator Pads 2346N · Class 2

Adverse event reports
1
Deaths reported
1
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387284740), received between Sep 26, 2017 and Sep 26, 2017 — classified as 1 death.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Operates Differently Than Expected1
  • Electrical /Electronic Property Problem1
  • Failure to Conduct1

Patient problems

  • Cardiac Arrest1
  • Death1
  • Sudden Cardiac Death1

Recent adverse event reports

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

  • DeathSep 26, 2017Failure to Conduct; Electrical /Electronic Property Problem; Device Operates Differently Than Expected; Failure to Conduct; Electrical /Electronic Property Problem; Device Operates Differently Than Expected

    NEW INFORMATION: IT WAS REPORTED THAT THE PATIENT WAS GIVEN TWO SHOCKS USING THE SAME PADS WITH TWO DIFFERENT DEFIBRILLATORS.

    Patient problems: Cardiac Arrest; Death; Sudden Cardiac Death

    MAUDE report 6896043 ↗

Other MEDIA, ELECTROCONDUCTIVE devices

All MEDIA, ELECTROCONDUCTIVE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.