BOVIE A1252CRecalls & reported problems
Aspen Surgical Products, Inc. · REUSABLE GROUNDING CABLE · Class 2
All models of Bovie (42)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10607151001541), received between Dec 18, 2018 and Jun 21, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Grounding Malfunction” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Grounding Malfunction1
- Output Problem1
Patient problems
- Burn(s)1
- Burn, Thermal1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 21, 2024Grounding Malfunction; Output Problem; Grounding Malfunction; Output Problem
THE COMPLAINANT ALLEGES, "BURNED ON THE FINGER WHEN USING THE A952 GENERATOR WITH A1252C CABLE. CABLE DID NOT GROUND CORRECTLY. NO PATIENT INVOLVEMENT. PHYSICIAN INVOLVEMENT (MINOR BURN)".
Patient problems: Burn(s)
MAUDE report 19589129 ↗MalfunctionDec 18, 2018Adverse Event Without Identified Device or Use Problem
THE CUSTOMER ALLEGED THAT DURING A PROCEDURE, THE PATIENT WAS BURNED BY THE CORD THAT ATTACHES TO THE SPLIT PAD.
Patient problems: Burn, Thermal
MAUDE report 8176498 ↗
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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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