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Megadyne 0036HBNRecalls & reported problems

Megadyne Medical Products, Inc. · Electrosurgical Pencil Rocker Switch E-Z Clean Coated Modified Blade Electrode 10 ft (3 m) cord Holster Bulk Non Sterile · 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 10614559103531), received between Oct 14, 2021 and Oct 14, 2021 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Full thickness (Third Degree) Burn1

Recent adverse event reports

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

  • InjuryOct 14, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT DURING A BREAST AUGMENTATION A PATIENT INCIDENT OCCURRED WHILE USING SUPPLIES FROM A CUSTOM PACK. THE PACK IS THE PLASTIC PACK THE PHYSICIAN WAS USING THE CAUTERY ON A PATIENT WHEN THE CAUTERY BURNED THE PATIENT¿S SKIN. THE ITEM IN THE PACK THAT BURNT THE PATIENT WAS PENCIL CAUTERY WITH HOLSTER.

    Patient problems: Full thickness (Third Degree) Burn

    MAUDE report 12633238 ↗

Other ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES devices

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Sources and updates

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