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Megadyne ME725M1ERecalls & reported problems

Megadyne Medical Products, Inc. · MEGADYNE ACE BLADE 700, 2.5" Modified Blade, PTFE Coated, ZIP Pen Smoke Evacuation Pencil, E Connector, 10 Ft (3.04m) Tubing · Class 2

Data updated Oct 18, 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 10614559105672), received between Mar 16, 2023 and Mar 16, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMar 16, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS REPORTED PRE-OP THE THE BREAST MASS EXCISION PROCEDURE THAT WHEN OPENING THE PRODUCT ONTO THE BACK TABLE, THE BLACK SLEEVE THAT MAKES THE BLADE, A MODIFIED TIP, CAME OFF. THIS HAPPENED PRIOR TO THE CASE WE OPENED A NEW DEVICE. THERE WERE NO PATIENT CONSEQUENCES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16554303 ↗

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Sources and updates

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