Kangaroo 461701Recalls & reported problems

Cardinal Health 200, LLC · Radiopaque Line, Safe Enteral Connections · Class 2

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521067981), received between Nov 6, 2017 and Nov 6, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Overheating of Device” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

Overheating of Device1

Patient problems

No Patient Involvement1

Recent adverse event reports

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

MalfunctionNov 6, 2017Overheating of Device; Overheating of Device
ACCORDING TO THE INITIAL REPORTER, NURSING CLAIMED THAT THE CONNECTOR CAME APART FROM THE FEEDING TUBE REQUIRING THE EXISTING DEVICE TO BE REMOVED AND A NEW FEEDING TUBE PLACED. NO PATIENT INJURY.
Patient problems: No Patient Involvement
MAUDE report 7003634 ↗

Device details

UDI-DI	`10884521067981`
Brand	Kangaroo
Model	461701
Company	Cardinal Health 200, LLC
Product code	KNT · TUBES, GASTROINTESTINAL (AND ACCESSORIES)
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	Not in Commercial Distribution
Record updated	Feb 24, 2026

Device type (GMDN): Nasoenteral tube

A sterile, thin, flexible, hollow cylinder designed to access the small intestines (duodenum or jejunum) through the nose and nasopharynx for examination (e.g., of intestinal contents), treatment (e.g., decompression, short-term feeding), or other purposes. It is a single- or dual-lumen, rubber or plastic tube (nasoduodenal or nasojejunal tube) that is smaller and longer than a nasogastric tube and may have a small weight or magnet at the distal tip to facilitate placement. It is frequently used for very ill or comatose patients. Some types are used to remove air and liquids from the stomach by connection to intermittent suction units and/or for enteral feeding. This is a single-use device.

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.