KangarooRecalls & reported problems across all models
Cardinal Health 200, LLC · 35 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 130
- Deaths reported
- 1
- Injuries reported
- 28
- Recalls
- 0
We found 35 models of Kangaroo by Cardinal Health 200, LLC in the FDA's device registry (GUDID). Together they are named in 130 adverse event reports in the FDA's MAUDE database, received between Nov 6, 2017 and Sep 16, 2026 — classified as 1 death, 28 injuries, 101 malfunctions.
The most frequently reported specific device problem is “Air/Gas in Device” (24 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Kangaroo problems
Device problems
- Air/Gas in Device24
- Detachment of Device or Device Component21
- Break14
- Unintended Deflation14
- Infusion or Flow Problem9
- Material Separation9
- Insufficient Flow or Under Infusion7
- Disconnection5
Patient problems
- No Clinical Signs, Symptoms or Conditions64
- No Consequences Or Impact To Patient19
- No Known Impact Or Consequence To Patient9
- Hypoglycemia7
- Dehydration6
- Hypernatremia4
- Insufficient Information3
- No Patient Involvement3
Kangaroo models
35 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Kangaroo 385400Pump, infusion, enteral1 death27 reports
- Kangaroo 8884720247Tubes, gastrointestinal (and accessories)14 reports
- Kangaroo 461438TUBES, GASTROINTESTINAL (AND ACCESSORIES)9 reports
- Kangaroo 773662Pump, infusion, enteral8 reports
- Kangaroo 461355TUBES, GASTROINTESTINAL (AND ACCESSORIES)8 reports
- Kangaroo 461412TUBES, GASTROINTESTINAL (AND ACCESSORIES)7 reports
- Kangaroo 461420TUBES, GASTROINTESTINAL (AND ACCESSORIES)6 reports
- Kangaroo 461503TUBES, GASTROINTESTINAL (AND ACCESSORIES)6 reports
- Kangaroo 461055ETubes, gastrointestinal (and accessories)4 reports
- Kangaroo 773656Pump, infusion, enteral3 reports
- Kangaroo 8884720205Tubes, gastrointestinal (and accessories)3 reports
- Kangaroo B5FDPump, infusion, enteral3 reports
- Kangaroo BSPFFPump, infusion, enteral3 reports
- Kangaroo E10FDRPump, infusion, enteral3 reports
- Kangaroo 8884705008EPump, infusion, enteral2 reports
- Kangaroo 60ENSGastrointestinal Tubes with Enteral Specific Connectors2 reports
- Kangaroo BSPFDPump, infusion, enteral2 reports
- Kangaroo 461800TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 reports
- Kangaroo B10FDPump, infusion, enteral2 reports
- Kangaroo 461043ETubes, gastrointestinal (and accessories)1 report
- Kangaroo 461243ETubes, gastrointestinal (and accessories)1 report
- Kangaroo 461412Tubes, gastrointestinal (and accessories)1 report
- Kangaroo 461420EGastrointestinal Tubes with Enteral Specific Connectors1 report
- Kangaroo 461438Tubes, gastrointestinal (and accessories)1 report
- Kangaroo 461503EGastrointestinal Tubes with Enteral Specific Connectors1 report
- Kangaroo 762010ETubes, gastrointestinal (and accessories)1 report
- Kangaroo 772055Pump, infusion, enteral1 report
- Kangaroo 8884702500Tubes, gastrointestinal (and accessories)1 report
- Kangaroo 8884715148Tubes, gastrointestinal (and accessories)1 report
- Kangaroo 8884720221Tubes, gastrointestinal (and accessories)1 report
- Kangaroo 60ENYGastrointestinal Tubes with Enteral Specific Connectors1 report
- Kangaroo 461701TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Kangaroo B10FFPump, infusion, enteral1 report
- Kangaroo BSPFDPump, infusion, enteral1 report
- Kangaroo E5FDRPump, infusion, enteral1 report
Recent Kangaroo adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Air/Gas in Device
The customer reported the pump did not stop at the end of the feed and after the bag was empty it created air in the tube. The customer admitted he had the pump for one year and never cleaned it or the sensors. The customer was educated on cleaning the pump and sensors.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50787505 ↗MalfunctionSep 4, 2026Air/Gas in Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50610049 ↗MalfunctionAug 28, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50497543 ↗InjuryJun 24, 2026Improper Flow or Infusion
THE CUSTOMER REPORTED THAT THE CHILD HAD BEEN USING THE PUMP FOR A WHILE AND WHEN THE MOM REALIZED THE DEVICE WAS NOT INFUSING, HE WAS ADMITTED TO THE HOSPITAL. THE REASON THE CHILD WAS ADMITTED TO THE HOSPITAL AND THE MEDICAL INTERVENTION REQUIRED IS UNKNOWN.
Patient problems: Insufficient Information
MAUDE report 25608578 ↗MalfunctionJun 8, 2026Unintended Deflation
THE CUSTOMER REPORTED WHEN INFLATING THE BALLOON, IT WAS PUNCTURED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25429286 ↗MalfunctionMay 18, 2026Break
THE CUSTOMER REPORTED A TEAR IN THE INSERTED PORTION OF THE NG TUBE WHICH WAS NOTED WHEN THE TUBE WAS REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25209134 ↗MalfunctionMay 6, 2026Air/Gas in Device
THE CUSTOMER REPORTED THE TEAM HAS BEEN REPORTING AN INCREASE IN "CASSETTE SLIPPED" AND "CASSETTE ERROR" ALARMS. STAFF ARE NOTICING INCREASED AIR IN THE LINE, DESCRIBED AS THE FORMULA RUNNING DOWN ONE SIDE OF THE TUBING INSTEAD OF FULLY OCCUPYING THE LINE, WITH THE FORMULA FILING ONLY PART OF THE TUBING RATHER THAT THE ENTIRE LUMEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25093546 ↗MalfunctionMay 1, 2026Material Separation
THE CUSTOMER REPORTED THE PATIENT ATTEMPTED TO PULL OUT THE IRIS TUBE AND THE NURSE INTERVENED BY GRASPING THE TUBE NEAR THE NARE TO PREVENT REMOVAL OF BOTH THE TUBE AND THE BRIDLE. DURING THIS EVENT, THE TUBE SPLIT AT THE 84CM MARK BETWEEN THE POINT WHERE THE NURSE WAS HOLDING IT AND WHERE THE PATIENT WAS PULLING. NO HARM TO THE PATIENT REPORTED. PER ADDITIONAL INFORMATION PROVIDED, THE REMAINDER OF THE TUBE WAS REMOVED BY HAND, NO ADDITIONAL PROCEDURES WERE PERFORMED. A NEW TUBE WAS NOT PLACED AFTER THE REMOVAL OF THIS TUBE AS THE PATIENT WAS COMBATIVE AND THE MEDICAL TEAM OPTED NOT TO REINSERT ANOTHER TUBE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25057542 ↗MalfunctionApr 27, 2026Material Separation
THE CUSTOMER REPORTED THE NURSE WENT TO ADJUST THE TAPE AND THE NG TUBE SNAPPED IN HALF. THE TUBE HAD TO BE REPLACED. PER ADDITIONAL INFORMATION PROVIDED ON (B)(6) 2026, THE NG FEEDING TUBE WAS REMOVED BY HAND AND REPLACED WITH A NEW NG TUBE. NO SPECIAL PROCEDURE NEEDED TO BE PERFORMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25003920 ↗MalfunctionApr 17, 2026Break
THE CUSTOMER REPORTED THE IRIS TUBE WAS BEING REMOVED AND THE NURSE NOTICED A BREAK IN THE TUBING. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24916319 ↗MalfunctionApr 16, 2026Break
THE CUSTOMER REPORTED A NURSE HAD AN ISSUE WHILE SETTING UP A REFEED OF INFUSION FOR A PATIENT. THE CONNECTOR TUBING BROKE AT THE Y-CONNECTION SITE WHILE THE NURSE WAS TRYING TO CONNECT IT TO THE PATIENT. THE NURSE WAS ABLE TO GET ANOTHER SET OF TUBING TO USE FOR THE REFEED. THERE WAS VERY LITTLE OF THE REFEED LOST DUE TO THE BROKEN SET. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24903202 ↗MalfunctionApr 13, 2026Break
THE CUSTOMER REPORTED THE ITEM IS NOT WORKING AND HAS HOLES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24860123 ↗MalfunctionApr 1, 2026Break
THE CUSTOMER REPORTED THE MIDDLE OF ONE OF THE PORTS ON THE EXTENSION FOR THE G-TUBE BROKE OFF. THE CUSTOMER WAS NOT ABLE TO CLOSE THE PORT WHEN IT WAS NOT IN USE. IT POSSIBLY BROKE OFF DUE TO ATTACHING TO THE PORT TOO TIGHTLY, BUT THEY HAVE NEVER SEEN ONE BREAK OFF AT THAT SPOT BEFORE. NO HARM WAS DONE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24752980 ↗MalfunctionMar 18, 2026Air/Gas in Device
THE CUSTOMER REPORTED DURING TESTING THE PUMP KEPT ALARMING AND AIR WAS OBSERVED IN THE LINE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24625954 ↗MalfunctionMar 16, 2026Unintended Deflation
THE CUSTOMER REPORTED THEY HAVE RECENTLY OBSERVED AN INCREASED INCIDENCE OF BALLOON RUPTURE RESULTING IN TUBE DISLODGEMENT. PER ADDITIONAL INFORMATION PROVIDED ON 13MAR2026, AN INCIDENCE OF A BALLOON RUPTURE OCCURRED ON (B)(6) 2025 AT 1300HR. THE G-TUBE WAS FOUND DISLODGED WITH THE BALLOON RUPTURED, AND WAS REPLACED WITH ANOTHER G-TUBE, ITEM CODE: 8884720221E, NOT 8884720221.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24610970 ↗
Other Cardinal Health 200, LLC products
- JACKSON-PRATT20 models · 13 reports · 19 recalls
- Monoject35 models · 96 reports · 11 recalls
- CONVERTORS38 models · 40 reports · 11 recalls
- Argyle33 models · 58 reports · 7 recalls
- Salem Sump31 models · 40 reports · 7 recalls
- Dover45 models · 241 reports · 2 recalls
- Kendall31 models · 51 reports · 3 recalls
- NOVAPLUS7 models · 75 reports · 1 recall
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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