3M™ 1149C-LPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50707387580716), received between May 22, 2019 and May 22, 2019 — classified as 1 injury.

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

Recent adverse event reports

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

• InjuryMay 22, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A REGISTERED NURSE (RN) REPORTED THAT A 3M¿ UNIVERSAL ELECTROSURGICAL PAD (1149C-LP) WAS APPLIED TO A PATIENT'S RIGHT ANTERIOR/LATERAL THIGH DURING A BODYTITE ABDOMINAL AND FACETITE FACE AND NECK SURGICAL PROCEDURES WITH BILATERAL EXCISION OF AXILLA DOGEARS. THE PATIENT WAS IN SUPINE POSITION DURING THE PROCEDURE. THE RN INFORMED THAT TOWARD END OF PROCEDURE, A CAUTERY PENCIL, PUSH-BUTTON STAINLESS-STEEL BLADE, STOPPED WORKING, AND AFTER THE ELECTROCAUTERY PENCIL WAS REPLACED, THE GROUNDING PLATE WAS CHECKED AND THE BURN WAS IDENTIFIED AT THAT TIME. THE RN ALLEGED THAT A 2CM X 2CM 3RD DEGREE THERMAL BURN OCCURRED UNDER THE CAUTERY GROUNDING PAD. TREATMENT CONSISTED OF PRIMARY EXCISION AND CLOSURE. THE PATIENT IS REPORTED TO BE HEALING WELL.

  Patient problems: Full thickness (Third Degree) Burn

  MAUDE report 8633808 ↗