Bovie A802EURecalls & reported problems
Aspen Surgical Products, Inc. · REUSABLE GROUNDING PAD WITH CABLE · Class 2
All models of Bovie (42)
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 10607151001534), received between Feb 15, 2022 and Feb 15, 2022 — classified as 1 malfunction.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Electric Shock1
- Superficial (First Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 15, 2022Adverse Event Without Identified Device or Use Problem
THE CUSTOMER ALLEGED THAT WHILE USING THE A952 WITH THE A802EU, THE PHYSICIAN IS RECEIVING SHOCKS OF ELECTRICITY AND THE PATIENT IS RECEIVING SLIGHT BURNING/PAIN IN THEIR EYES. THERE WAS NO SIGNIFICANT DAMAGE TO THE USER OR THE PATIENT.
Patient problems: Electric Shock; Superficial (First Degree) Burn
MAUDE report 13536380 ↗
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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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