3M™ 8180F (UDI 10707387802919)Recalls & reported problems
3m Company · 3M™ Electrosurgical Pad, 8180F, Large Split Non-Corded, 5 Each/Bag, 5 Bag/Pack, 8 Pack/Case, for Stryker · Class 2
Data updated Oct 16, 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 10707387802919), received between Jun 5, 2023 and Jun 5, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Human-Device Interface Problem” (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
- Human-Device Interface Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 5, 2023Human-Device Interface Problem; Human-Device Interface Problem
A 75-YEAR-OLD MALE ALLEGEDLY EXPERIENCED A LEFT LATERAL MID-THIGH 6X4 CM 2ND DEGREE BURN WITH THE USE OF THE 3M¿ ELECTROSURGICAL PATIENT PLATES 8180F, LOT: 202510MV, AND SUBSEQUENTLY UNDERWENT DEBRIDEMENT OF THE NECROTIC TISSUE.
Patient problems: Burn(s)
MAUDE report 17064063 ↗
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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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