Kangaroo 461420Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10884521067936), received between Nov 12, 2019 and Aug 11, 2022 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 11, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THAT THE END OF THE FEEDING TUBE (WHERE THE SYRINGE ATTACHES) CAME OFF OF THE TUBE WHEN THE RN WAS REMOVING THE TUBE FROM THE INFANT. PER ADDITIONAL INFORMATION RECEIVED ON (B)(6) 2022, THERE WAS NO MEDICAL INTERVENTION REQUIRED. AND THERE WAS NO INJURY REPORTED. THEY HAD THE TUBE REPLACED. THE ENTIRE DEVICE WAS RETRIEVED, NO PIECES WERE LEFT IN THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15214069 ↗
• MalfunctionMar 15, 2022Fluid/Blood Leak; Detachment of Device or Device Component; Fluid/Blood Leak; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THAT THE PORT OF THE FEEDING TUBE WAS DISCONNECTING FROM THE TUBE AND THERE WAS LEAKING. THE TUBE WAS REMOVED AND SAVED. AFTERWARD, THE PORT SEPARATED FROM THE TUBE COMPLETELY. THE TUBE WAS SWAPPED OUT FOR A NEW TUBE WHICH WORKED WITHOUT ISSUE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13773693 ↗
• MalfunctionJan 14, 2020Material Separation; Material Separation

  THE CUSTOMER REPORTED THE FEEDING TUBE WAS PUT IN AND CAME APART WHILE BEING USED RIGHT THEN. THE PURPLE HUB AT THE TOP WHERE THE SYRINGE ATTACHES ACTUALLY DETACHED FROM THE TUBE THAT GOES INTO THE PATIENT. THE TUBE WAS JUST PUT INTO THE PATIENT AND IT WAS THE FIRST TIME THAT IT WAS GOING TO BE USED WHEN THE PURPLE HUB DETACHED FROM THE TUBING. THE TUBE WAS IMMEDIATELY TAKEN OUT OF THE PATIENT AND REPLACED WITH A NEW ONE. THERE WAS NO HARM TO THE PATIENT AS THE TUBE WAS TAPED WELL AND THE NURSES WERE QUICK IN REMOVING IT FROM THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9586826 ↗
• MalfunctionJan 14, 2020Material Separation; Material Separation

  THE CUSTOMER REPORTED THE FEEDING TUBE WAS IN PLACE FOR LESS THAN 24 HOURS WHEN IT CAME APART. THE PURPLE HUB AT THE TOP WHERE THE SYRINGE ATTACHES ACTUALLY DETACHED FROM THE TUBE THAT GOES INTO THE PATIENT. THE TUBE WAS IMMEDIATELY TAKEN OUT OF THE PATIENT AND REPLACED WITH A NEW ONE. THERE WAS NO HARM TO THE PATIENT AS THE TUBE WAS TAPED WELL AND THE NURSES WERE QUICK IN REMOVING IT FROM THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9586732 ↗
• MalfunctionNov 12, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THAT THE HUB SEPARATED FROM THE TUBING.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9312716 ↗
• MalfunctionNov 12, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THAT THE HUB SEPARATED FROM THE TUBING.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9312712 ↗