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BOVIE ULTIMATE BVX-100HRecalls & reported problems

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

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10607151009769), received between Oct 31, 2018 and Oct 31, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

Most reported problems

Device problems

  • Device Dislodged or Dislocated1
  • Grounding Malfunction1
  • Use of Device Problem1

Patient problems

  • Burn(s)1
  • Patient Problem/Medical Problem1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 31, 2018Grounding Malfunction; Use of Device Problem; Device Dislodged or Dislocated; Grounding Malfunction; Use of Device Problem; Device Dislodged or Dislocated

    A PATIENT SUFFERED FROM A BURN FROM A GROUNDING PAD DURING A SURGICAL PROCEDURE.

    Patient problems: Burn(s); Patient Problem/Medical Problem

    MAUDE report 8025386 ↗

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Sources and updates

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