DUALTO Energy System ETHUSCRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20705036038372), received between Aug 14, 2026 and Aug 14, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Arcing of Electrodes” (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 18, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryAug 14, 2026Arcing of Electrodes; Adverse Event Without Identified Device or Use Problem

  It was reported that, during a total laparoscopic hysterectomy with bilateral salpingectomy for uterine fibroids, bleeding from the port site was cauterized using a right-angle electrode of the Probe Plus during wound closure. An electric current ran through the muscle retractor that was placed in the surgical field at that time, causing a second-degree burn. The attending physician's opinion is that it may have been an electrical discharge. The patient is female, but it is currently confirming the treatment she received for this incident, her condition after treatment, and the patient background information. No further information is available.

  Patient problems: Partial thickness (Second Degree) Burn

  MAUDE report 50255811 ↗