HYFRECATOR 7-900-230Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20653405031618), received between Apr 17, 2023 and Apr 17, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended Electrical Shock” (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.

• MalfunctionApr 17, 2023Unintended Electrical Shock; Unintended Electrical Shock

  THE DISTRIBUTOR REPORTED ON BEHALF OF THE CUSTOMER THAT THE 7-900-230, HYFRECATOR 2000, 230V DURING PRE-OPERATIVE CHECK ON 27MAR23 SHOCKED A STAFF MEMBER, ¿NO PATIENT PLATE WAS BEING USED.¿. THE PROCEDURE WAS NOT COMPLETED AND THERE WAS NO DELAY REPORTED. AN ALTERNATE DEVICE WAS NOT USED. AFTER FURTHER ASSESSMENT IT WAS FOUND, "THERE WAS NO INJURY TO THE DOCTOR. THERE WAS NO MEDICAL/SURGICAL INTERVENTION REQUIRED FOR THE DOCTOR. THE DOCTOR IS OK". THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE

  Patient problems: Electric Shock

  MAUDE report 16751068 ↗