Kangaroo 762000Recalls & reported problems
Cardinal Health, Inc. · Safety Single Pass PEG Kit,Pull · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 40884521020161), received between Oct 26, 2017 and Mar 7, 2018 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment Of Device Component” (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
- Detachment Of Device Component1
- Device Contamination with Chemical or Other Material1
- Difficult to Remove1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 7, 2018Difficult to Remove; Device Contamination with Chemical or Other Material; Difficult to Remove; Device Contamination with Chemical or Other Material
THE CUSTOMER REPORTED THAT WHILE EXTERNALIZING THE TUBE THROUGH THE ABDOMINAL WALL, THE TUBE DOES NOT PASS AND THE DISTAL MATERIAL IS LOST.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7320915 ↗InjuryOct 26, 2017Detachment Of Device Component; Detachment Of Device Component
ACCORDING TO THE REPORTER, DURING A LAPAROTOMY ON (B)(6) 2017 FOR DRAINAGE OF HEMOPERITENE, GASTRORRHAPHY, GASTROSTOMY, THE DEVICE GUIDE BROKE THE HANDLE OF THE WIRE DURING EXTRACTION. THERE WAS AN EXTENSION OF HOSPITALIZATION DUE TO REMOVAL OF GUIDE WIRE VIA SURGERY. THE PATIENT STATUS WAS UNKNOWN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6980042 ↗
Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices
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- CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)1 recall22 deaths134 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000720Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death170 reports
- EndoVive Safety PEG Kit M00566470Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 recall1 death111 reports
- Kangaroo 8884711253Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)152 reports
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 reports
- NutraGlide Nasal Feeding Tube ENFT-05055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.