Crossfire 0475000000Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327058086), received between Nov 28, 2018 and May 9, 2023 — classified as 1 injury, 3 malfunctions.

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 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 9, 2023Activation Failure; Activation Failure

  IT WAS REPORTED THAT THE PROCEDURE WAS CANCELLED. THE PATIENT WAS UNDER ANESTHESIA, BUT NO INCISION WAS MADE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16898803 ↗
• InjuryJul 23, 2019Adverse Event Without Identified Device or Use Problem

  MULTIPLE ATTEMPTS WERE MADE FOR ADDITIONAL INFORMATION, HOWEVER NO INFORMATION WAS RECEIVED. IT WAS REPORTED THAT THE DEVICE MALFUNCTIONED RESULTING IN INJURY TO THE PATIENT.

  Patient problems: Injury

  MAUDE report 8817828 ↗
• MalfunctionMar 28, 2019Insufficient Device Problem Information

  IT WAS REPORTED THAT THERE WAS A THERMAL EVENT WITH THE PRODUCT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8461272 ↗
• MalfunctionNov 28, 2018Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THERE WAS A THERMAL EVENT. PER ADDITIONAL INFORMATION RECEIVED, THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A REPLACEMENT DEVICE WITH NO REPORTS OF ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION.

  Patient problems: Burn, Thermal

  MAUDE report 8112757 ↗