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UtahLoop LETZ ElectrodeRecalls & reported problems

Utah Medical Products, Inc. · Electrosurgical Loop Electrode, 25mm Wide X 22mm Deep, Round Loop, 11cm Shaft Length, with Safe-T-Gauge · Class 2

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 H671DLPE110), received between Jul 13, 2023 and Jul 13, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Failure to Cut” (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

  • Failure to Cut1

Patient problems

  • Unspecified Tissue Injury1

Recent adverse event reports

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

  • InjuryJul 13, 2023Failure to Cut; Failure to Cut

    ON (B)(6) 2023 UTMD RECEIVED A MEDWATCH REPORT NUMBER MW5118217 WITH THE EVENT DESCRIPTION "DURING LEEP PROCEDURE, EQUIPMENT FAILED CUTTING AND CAUTERIZING AFTER INCISION RESULTING IN INJURY TO PT".

    Patient problems: Unspecified Tissue Injury

    MAUDE report 17316623 ↗

Other Electrosurgical, Cutting & Coagulation & Accessories devices

All Electrosurgical, Cutting & Coagulation & Accessories devices →

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