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Megadyne 0030HBNRecalls & reported problems

Megadyne Medical Products, Inc. · Electrosurgical Pencil Rocker Switch E-Z Clean Coated Blade Electrode 10 ft (3 m) cord Holster Bulk Non Sterile · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
6
Deaths reported
0
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10614559101322), received between Oct 15, 2018 and Oct 15, 2018 — classified as 6 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem5
  • Insufficient Device Problem Information1

Patient problems

  • Unspecified Infection6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 15, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE DOCTOR PERFORMED A CRANIOTOMY ON A PATIENT AND AFTER THE PROCEDURE, THE PATIENT RETURNED WITH AN INFECTION. IT WAS NOT REPORTED HOW THE INFECTION WAS TREATED.

    Patient problems: Unspecified Infection

    MAUDE report 7966614 ↗
  • InjuryOct 15, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE DOCTOR PERFORMED A CRANIOTOMY ON A PATIENT AND AFTER THE PROCEDURE, THE PATIENT RETURNED WITH AN INFECTION. IT WAS NOT REPORTED HOW THE INFECTION WAS TREATED.

    Patient problems: Unspecified Infection

    MAUDE report 7966606 ↗
  • InjuryOct 15, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE DOCTOR PERFORMED A CRANIOTOMY ON A PATIENT AND AFTER THE PROCEDURE, THE PATIENT RETURNED WITH AN INFECTION. IT WAS NOT REPORTED HOW THE INFECTION WAS TREATED.

    Patient problems: Unspecified Infection

    MAUDE report 7966589 ↗
  • InjuryOct 15, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE DOCTOR PERFORMED A CRANIOTOMY ON A PATIENT AND AFTER THE PROCEDURE, THE PATIENT RETURNED WITH AN INFECTION. IT WAS NOT REPORTED HOW THE INFECTION WAS TREATED.

    Patient problems: Unspecified Infection

    MAUDE report 7966517 ↗
  • InjuryOct 15, 2018Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE DOCTOR PERFORMED A CRANIOTOMY ON A PATIENT AND AFTER THE PROCEDURE, THE PATIENT RETURNED WITH AN INFECTION. IT WAS NOT REPORTED HOW THE INFECTION WAS TREATED.

    Patient problems: Unspecified Infection

    MAUDE report 7966489 ↗
  • InjuryOct 15, 2018Insufficient Device Problem Information

    IT WAS REPORTED THAT THE DOCTOR PERFORMED A CRANIOTOMY ON A PATIENT AND AFTER THE PROCEDURE, THE PATIENT RETURNED WITH AN INFECTION. IT WAS NOT REPORTED HOW THE INFECTION WAS TREATED.

    Patient problems: Unspecified Infection

    MAUDE report 7966444 ↗

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Sources and updates

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