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Bovie A2250-LOANERRecalls & reported problems

Aspen Surgical Products, Inc. · AARON 2250-LOANER HIGH FREQUENCY ELECTROSURGICAL GENERATOR · Class 2

All models of Bovie (42)

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 10607151002784), received between Aug 9, 2023 and Aug 9, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (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

  • Use of Device Problem1

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.

  • MalfunctionAug 9, 2023Use of Device Problem; Use of Device Problem

    THE CUSTOMER ALLEGED THAT WHILE USING AN A2250, THE PATIENT FELT A TINGLING UNDER THE PAD BEING USED. THE USER HAD TO STOP THE PROCEDURE TWICE TO CHECK UNDER THE PAD WHICH DELAYED THE PROCEDURE. THE A2250 WAS REMOVED FROM THE SURGERY AND AN AA03 - HANDHELD CAUTERY WAS USED IN ITS PLACE. NO FURTHER HARM TO THE CUSTOMER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17490385 ↗

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Sources and updates

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