Kangaroo 721088CNRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521033617), received between Jul 13, 2020 and Jul 23, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Remove” (2 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 23, 2020Difficult to Remove; Difficult to Remove

  THE CUSTOMER REPORTED THE PATIENT WAS ADMITTED FROM THE EMERGENCY DEPARTMENT (ED) AND WHEN THEY ARRIVED TO THE INTENSIVE CARE UNIT, THE GUIDE WIRE WOULDN¿T COME OUT OF THE TUBE. THERE WAS NO HARM TO THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10313580 ↗
• MalfunctionJul 13, 2020Difficult to Remove; Difficult to Remove

  THE CUSTOMER REPORTED THAT THE FEEDING TUBE WAS INSERTED AND THE GUIDEWIRE WOULD NOT COME OUT. THE NURSE CALLED THE NURSE MANAGER OVER AND THEY REMOVED THE TUBE BUT THE GUIDEWIRE REMAINED STUCK IN THE TUBE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10264599 ↗