Intelliflow 700-102941Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI H7877001029410), received between Oct 23, 2023 and Oct 23, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).

1 other recall cover devices cleared under the same FDA submission (K040989); they may or may not involve this specific model.

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

• MalfunctionOct 23, 2023Fluid/Blood Leak; Fluid/Blood Leak

  INTELLIFLOW PUMP: AN ANGIODYNAMICS TERRITORY MANAGER REPORTED A FEW "ISSUES." IT WAS, REPORTEDLY, HARD TO TELL IF THE ISSUES WERE THE 25CM TALON SEMIFLEX PROBES OR A COMBINATION OF PROBES AND THE INTELLIFLOW PUMP, OR THE RFA UNIT. THE ACCOUNT INDICATED THAT WATER WAS EVERYWHERE BUT THEY NOTICED NO HOLES IN THE TUBING. ULTIMATELY, THE PROCEDURE WAS COMPLETED WITH A THIRD PROBE. THERE WAS NO HARM EXPERIENCED BY THE PATIENT; HOWEVER, THE CASE WAS DELAYED OVER AN HOUR WHILE THE PATIENT WAS UNDER GENERAL ANESTHESIA. THIS EVENT MEETS THE CRITERIA A REPORTABLE ADVERSE EVENT; PATIENT SAFETY RISK DUE TO PROLONGED PROCEDURE GREATER THAN 30 MINUTES (EXTENDED SEDATION).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17987046 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K040989. One submission often covers many models, so check the product and lot details in each record.

• Z-1675-2013 · Jun 11, 2013 · Terminated
  AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with the RITA RF Generators and RITA electrosurgical devices.