Kangaroo 8884711501Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884521009684), received between Sep 8, 2017 and Oct 17, 2022 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 17, 2022Complete Blockage; Complete Blockage

  THE CUSTOMER REPORTED THAT A DOCTOR INSERTED A NEW FEEDING TUBE INTO A PATIENT BUT WAS UNABLE TO ASPIRATE GASTRIC CONTENT FROM THE SIDE PORT. THE TUBE WAS THEN REMOVED FROM THE PATIENT AND THE USERS TRIED TO FLUSH BOTH PORTS AND REALIZE THAT THE SIDE PORT IS OCCLUDED, NEITHER AIR NOR WATER COULD BE FLUSHED THROUGH THE SIDE PORT. A NEW FEEDING TUBE FROM THE SAME LOT WAS OPENED AND INSERTED INTO SAME PATIENT AND BOTH PORTS IN THE NEWLY OPENED TUBE WAS WORKING WELL. NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15616016 ↗
• MalfunctionOct 17, 2022Complete Blockage; Complete Blockage

  THE CUSTOMER REPORTED THAT THE NURSE INSERTED A NEW FEEDING TUBE INTO THE PATIENT AND FED VIA THE MAIN PORT BUT THE SIDE PORT WAS OCCLUDED AS THE NURSE WAS UNABLE TO FLUSH/ASPIRATE FROM THE SIDE PORT. A NEW TUBE WAS OPENED AND INSERTED INTO SAME PATIENT AND BOTH PORTS WERE WORKING WELL. NO PATIENT INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15615910 ↗
• MalfunctionJul 23, 2019Fluid/Blood Leak; Fluid/Blood Leak

  THE CUSTOMER REPORTS THE FEEDING TUBE'S CAP FOUND LOOSE AFTER A FEW DAYS RESULTING IN THE LEAK OF THE FEEDING FORMULA.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8816945 ↗
• MalfunctionSep 8, 2017Leak/Splash; Leak/Splash

  THE CUSTOMER REPORTS THE NURSES EXPERIENCE LEAKAGE FROM THE PORT COVER WHILE USING IT. NURSES HAD TO SECURE TAPE TO HOLD THE PORT COVERS IN PLACE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6851497 ↗