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Edge E2450HDBNSBRecalls & reported problems

Covidien LP · Button Switch Pencil Blade Electrode, Holster; Caution: For manufacturing, processing, or repacking. · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884524002255), received between Jan 15, 2021 and Jan 15, 2021 — classified as 1 malfunction.

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

  • Adverse Event Without Identified Device or Use 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.

  • MalfunctionJan 15, 2021Adverse Event Without Identified Device or Use Problem

    ACCORDING TO THE REPORTER, THE USER'S THUMB HAD A BURN.

    Patient problems: Burn(s)

    MAUDE report 11177349 ↗

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Sources and updates

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