KangarooRecalls & reported problems across all models
Cardinal Health, Inc. · 145 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Kangaroo models — page 2
145 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Kangaroo 461701EGastrointestinal Tubes with Enteral Specific Connectors2 reports
- Kangaroo 771111EGastrointestinal Tubes with Enteral Specific Connectors2 reports
- Kangaroo 8884710867ETUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo 8884720817ETUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo 777702ETUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo 721088CNTubes, Gastrointestinal (And Accessories)2 reports
- Kangaroo 60EYTUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo 8884741813TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo 762000TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo 8884702500TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 712200TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 716120TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 718100TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 718120TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 718170TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 718230TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 718250TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 718400TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 720170TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 720300TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 724170TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 724250TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 724300TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884741220Tubes, Gastrointestinal (And Accessories)1 report
- Kangaroo 8884742035TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 674669Pump, infusion, enteral1 report
- Kangaroo 672027Pump, infusion1 report
- Kangaroo 8884752067TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 674668PUMP, INFUSION, ENTERAL1 report
- Kangaroo 710859CNTUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 384500CBCPUMP, INFUSION, ENTERAL1 report
- Kangaroo 8884710867TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884720855TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884721211TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884721237TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884752042TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 461503EGastrointestinal Tubes with Enteral Specific Connectors1 report
- Kangaroo 8884720841ETUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884720855ETUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884751622ETUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884752513TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 461055ETUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 461243ETUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death1 report
- Kangaroo 8884730774TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo 8884730790TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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