3M™ 2345NRecalls & reported problems
3m Company · 2345N DEFIB PAD, 10PKG/BX,10BX/CS · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 30707387284733), 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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
ADDITIONAL INFORMATION: APPLICATION OF A FIRST SET OF PATCHES (2345N) WAS PLACED ONTO THE PATIENT AND TWO EXTERNAL SHOCKS USING THE SAME DEFIBRILLATOR WAS GIVE TO THE PATIENT. NO SIGN OF CONDUCTION. ANOTHER SET OF PADS WERE APPLIED USING A DIFFERENT MODEL NUMBER.
Patient problems: Cardiac Arrest; Death; Sudden Cardiac Death
MAUDE report 6896056 ↗
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- 3M™ 2346N3m Company · MEDIA, ELECTROCONDUCTIVE1 death1 report
- SIGNAGEL ELECTRODE GELParker Laboratories Inc · Media, Electroconductive1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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