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
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 ↗
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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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