Kangaroo 773662 (UDI 10192253009958)Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10192253009958), received between Sep 13, 2023 and Mar 18, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Air/Gas in Device” (8 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• 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 ↗
• MalfunctionApr 18, 2024Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THERE WAS AN ERROR STATING THAT THERE WAS AIR IN THE LINE. ICU STAFF NOTED THE BAGS APPEAR TO BE SUCKING AIR INTO THE SYSTEM. PER ADDITIONAL INFORMATION PROVIDED, THE ISSUE OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT HARM. HOWEVER, IT IS DELAYING NUTRITION AND CAUSING SIGNIFICANT NURSING DELAYS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19137186 ↗
• MalfunctionApr 17, 2024Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THERE WAS AN ERROR STATING THAT THERE WAS AIR IN THE LINE. ICU STAFF NOTED THE BAGS APPEAR TO BE SUCKING AIR INTO THE SYSTEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19124444 ↗
• MalfunctionMar 19, 2024Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THEY ARE RECEIVING MULTIPLE ERRORS SUCH AS DOWNSTREAM OCCLUSION ERRORS, THE TUBES ARE LEAKING WATER, AND AIR IS GETTING INTO THE TUBING. PER ADDITIONAL INFORMATION PROVIDED ON 05MAR2024, THE CUSTOMER STATED THAT FROM THE NURSING REPORTS IT SOUNDS LIKE IT WAS EITHER LEAKING PRIOR TO PRIMING OR AFTER PRIMING, THE TUBES GOT AIR IN THEM, AND THAT CAUSED THE ERROR MESSAGES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18935682 ↗
• MalfunctionMar 6, 2024Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THEY ARE RECEIVING MULTIPLE ERRORS SUCH AS DOWNSTREAM OCCLUSION ERRORS, THE TUBES ARE LEAKING WATER, AND AIR IS GETTING INTO THE TUBING. PER ADDITIONAL INFORMATION PROVIDED ON (B)(6) 2024, THE CUSTOMER STATED THAT FROM THE NURSING REPORTS IT SOUNDS LIKE IT WAS EITHER LEAKING PRIOR TO PRIMING OR AFTER PRIMING, THE TUBES GOT AIR IN THEM, AND THAT CAUSED THE ERROR MESSAGES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18847335 ↗
• MalfunctionMar 6, 2024Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THEY ARE RECEIVING MULTIPLE ERRORS SUCH AS DOWNSTREAM OCCLUSION ERRORS, THE TUBES ARE LEAKING WATER, AND AIR IS GETTING INTO THE TUBING. PER ADDITIONAL INFORMATION PROVIDED ON (B)(6) 2024, THE CUSTOMER STATED THAT FROM THE NURSING REPORTS IT SOUNDS LIKE IT WAS EITHER LEAKING PRIOR TO PRIMING OR AFTER PRIMING, THE TUBES GOT AIR IN THEM, AND THAT CAUSED THE ERROR MESSAGES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18847321 ↗
• MalfunctionOct 24, 2023Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THAT THE PRODUCT KEEPS GETTING AIR IN THE BAGS AND WON'T LOSE THE AIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17995921 ↗
• MalfunctionSep 13, 2023Air/Gas in Device; Air/Gas in Device

  THE CUSTOMER REPORTED THAT THE NURSES HAVE BEEN HAVING ISSUES WITH THE KANGAROO PUMPS ALARMING AND FILLING WITH AIR IN THE TUBING. THIS HAS OCCURRED THROUGHOUT THE PAST TWO WEEKS. AFTER OBSERVATION AND NOT HAVING SUCCESS WITH KANGAROO PUMP CHANGES, IT LOOKS AS THOUGH THE ISSUE MAY BE WITH THE KANGAROO EPUMP SET WITH THE FLUSH BAG. THE ISSUE OCCURRING IS THAT THE PUMP WILL ALARM WITH A FLOW ERROR AND STAFF WILL THEN RE-PRIME THE BAG AND THE PUMP WILL STILL CONTINUE TO ALARM WITH THE SAME ERROR MESSAGE. THE OTHER SIGNIFICANT ISSUE IS THAT TUBING IS SOMEHOW FILLING WITH AIR ON THE SIDE CLOSEST TO THE PATIENT. THE AIR IN LINE ALARM ONLY OCCURS IF THE AIR DEVELOPS BEFORE THE MOTOR WHEEL, SO THIS MEANS AFTER THE MOTOR WHEEL THE TUBING IS FILLING WITH AIR. THIS COULD NEGATIVELY AFFECT THEIR POPULATION WITH DUODENAL TUBES BY PUTTING AIR IN THE BOWEL, AND ITS EASY TO MISS AS THIS ERROR WILL NOT TRIGGER A PUMP ALARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17738069 ↗