Megadyne 3030HRecalls & reported problems
Megadyne Medical Products, Inc. · E-Z Pen 12 Use Electrosurgical Pencil Rocker Switch 10 foot (3 m) cord Holster · Class 2
Data updated Oct 16, 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 10614559102527), received between Mar 6, 2019 and Mar 6, 2019 — classified as 1 malfunction.
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 16, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2019Insufficient Device Problem Information
IT WAS REPORTED DURING AN UNKNOWN PROCEDURE THE PATIENT RECEIVED TWO BURNS ON EITHER SIDE OF THE INCISION. THE BURNS WERE NOT LIFE THREATENING AND IT IS UNKNOWN HOW THE BURNS WERE TREATED. IT IS UNKNOWN HOW THE PROCEDURE WAS COMPLETED.
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 8395877 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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