Kangaroo 8884720205 (UDI 10192253011524)Recalls & reported problems
Cardinal Health 200, LLC · Gastrostomy Feeding Tube with Y-Ports · Class 2 · Implant
All models of Kangaroo (35)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10192253011524), received between May 7, 2025 and Dec 11, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Unintended Deflation” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Deflation2
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 11, 2025Break; Break
THE CUSTOMER REPORTED DURING THE PROCEDURE, THE GASTROSTOMY TUBE WAS DEFECTIVE ACCORDING TO THE MEDICAL TEAM. THE DOCTOR REPORTED THE TUBE HAD A HOLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23780916 ↗MalfunctionDec 11, 2025Unintended Deflation; Unintended Deflation
THE CUSTOMER REPORTED DURING THE PROCEDURE, THE GASTROSTOMY TUBE WAS DEFECTIVE ACCORDING TO THE MEDICAL TEAM. THE DOCTOR REPORTED THE TUBE HAD A DEFECT IN THE CUFF. PER ADDITIONAL INFORMATION PROVIDED BY THE CUSTOMER, THE BALLOON DEFLATED ON ITS OWN IN LESS THAN 30 DAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23780846 ↗MalfunctionMay 7, 2025Unintended Deflation; Unintended Deflation
THE CUSTOMER REPORTED THEY HAVE FOUND SOME ISSUES WITH G-TUBES THEY HAVE IN STOCK. THERE'S A LADY FROM THE NURSING HOME WHO HAD ONE REPLACED LAST WEEK AND IT CAME OUT. AND THEY SAW AN EMERGE YESTERDAY AND THE BALLOON WAS DEFECTIVE AND POPPED. THEY THEN INSERTED ANOTHER ONE AND FILLED THE BALLOON AND IMMEDIATELY IT POPPED AGAIN. THEY INSPECTED IT AND IT WAS THE BALLOON THAT WAS DEFECTIVE. THEY PLACED ANOTHER ONE BUT THEY ARE NOT SURE HOW DURABLE IT IS GOING TO BE. NO FURTHER INFORMATION WILL BE PROVIDED BY THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21976559 ↗
Other Tubes, gastrointestinal (and accessories) devices
- Bard® DigniShield® Stool Management System SMS002C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 deaths525 reports
- 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
- 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
- NutraGlide Nasal Feeding Tube ENFT-06055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page