Kangaroo 461055E (UDI 10192253007855)Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10192253007855), received between Oct 16, 2024 and May 18, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (3 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• 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 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 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 ↗
• MalfunctionOct 16, 2024Break; Break

  THE CUSTOMER REPORTED THAT DOBHOFF TUBE RUPTURED LONGITUDINALLY APPROXIMATE 2 CM IN LENGTH. ENTERAL FEEDS WERE REFLUXING OUT OF THE PATIENT'S LEFT NARE. PER CUSTOMER, THE TUBE WAS REMOVED AND REPLACED. ADDITIONAL INFORMATION WAS RECEIVED AND STATED THAT THERE WAS NO MEDICAL INTERVENTION OR TREATMENT PROVIDED. THE PATIENT IS DOING OK.

  Patient problems: Gastrointestinal Regurgitation

  MAUDE report 20464464 ↗