Skip to content

Bovie A1250SRecalls & reported problems

Aspen Surgical Products, Inc. · HIGH FREQUENCY ELECTROSURGICAL GENERATOR · Class 2

All models of Bovie (42)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00607151010263), received between May 28, 2024 and Jan 6, 2026 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Complete Loss of Power” (2 reports).

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 1 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 3 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Complete Loss of Power2
  • Failure to Power Up2
  • Intermittent Loss of Power1
  • Sparking1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6

Recent adverse event reports

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

  • MalfunctionJan 6, 2026Complete Loss of Power

    COMPLAINANT ALLEGES "ERROR CODE E-4 - WOULD NOT WORK DURING PROCEDURE".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23980337 ↗
  • MalfunctionDec 22, 2025Complete Loss of Power; Complete Loss of Power

    COMPLAINANT ALLEGES "ISSUE - DEVICE WIL SHUT OFF DURING USE."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23867530 ↗
  • MalfunctionDec 10, 2025Failure to Power Up; Failure to Power Up

    COMPLAINANT ALLEGES "ISSUE: UNIT IS CONNECTED PROPERLY, BUT NOT GETTING ANY CAUTERIZATION. TRIED MULTIPLE DIFFERENT ACTIVE CABLES AND GROUNDING PADS, BUT NOTHING WORKED."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23771379 ↗
  • MalfunctionDec 5, 2025Failure to Power Up; Failure to Power Up

    COMPLAINANT ALLEGES "NOT PUTTING OUT ANY POWER AT ALL."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23732714 ↗
  • MalfunctionNov 18, 2025Intermittent Loss of Power; Intermittent Loss of Power

    COMPLAINANT ALLEGES "PREVIOUSLY HAD A LEEP PROCEDURE WHERE THE MACHINE WASN'T CUTTING AS WELL AS IT USED TO A FEW WEEKS AGO SO SHE UPPED HER SETTINGS FROM 40/40 TO 50/50. THIS TIME, THE MACHINE STOPPED WORKING MID CUT. YOU COULD HEAR HER CUTTING THE TISSUE, THE MACHINE STOPPED ABRUPTLY WHILE SHE WAS STILL PRESSING THE BUTTON ON THE HAND CONTROLLER AND THEN IT STARTED UP AGAIN."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23586962 ↗
  • MalfunctionMay 28, 2024Sparking; Sparking

    THE COMPLAINANT ALLEGES, "TODAY THE MACHINE SPARKED FIRE (FLAME) FROM THE FRONT CONNECTION PLUG FOR THE FOOT CONTROL."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19410555 ↗

Other Electrosurgical, Cutting & Coagulation & Accessories devices

All Electrosurgical, Cutting & Coagulation & Accessories devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page