UltraVac 2110-10ECRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10614559104743), received between May 29, 2020 and May 29, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation Failure” (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.

• MalfunctionMay 29, 2020Activation Failure

  AFTER INCISION WAS MADE, BOVIE WAS ATTEMPTED TO USE AND DID NOT ACTIVATE ON FIELD. NO FAULT ALARMS ALERTED. GROUNDING PAD WAS CHECKED AND WAS IN THE GREEN. HAND PIECE AND GROUNDING PAD WERE DISCONNECTED AND RECONNECTED. NO ERROR MESSAGES, BUT STILL WOULD NOT ACTIVATE. A NEW HAND PIECE WAS OPENED, NO CHANGE. A NEW BOVIE PAD WAS PLACED ON THE PATIENT; NO CHANGE. A NEW MACHINE WAS BROUGHT IN THE ROOM AND BIO MED WAS CALLED. HAND PIECE STILL DID NOT WORK. BIO MED CHECKED THE MACHINE WITH A TEST HAND PIECE WHICH DID WORK CORRECTLY. BIO-MED SUGGESTED A NEW HAND PIECE FROM A DIFFERENT LOT NUMBER. A NEW LOT NUMBER WAS OPENED AND WORKED WITHOUT ISSUE ON BOTH MACHINES (COVIDIEN VALLEY LAB CONSOLES CN50920/CN50754). BOVIE SITE WAS CLEAR OF AN INJURY. NO HARM TO PATIENT WAS EVIDENT BUT DID CAUSE A DELAY INTRA-OPERATIVELY.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10100787 ↗