Kangaroo 8884752505 (UDI 10884521519022)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521519022), received between Jun 21, 2017 and Jul 23, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Complete Blockage” (1 report).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 23, 2021Difficult to Remove; Difficult to Remove

  THE CUSTOMER REPORTED A (B)(6) YEAR OLD FEMALE PATIENT WAS REFERRED BY HER ATTENDING PHYSICIAN FOR JAUNDICE ASSOCIATED WITH ALTERED GENERAL CONDITION WITH ANOREXIA FOR 1 WEEK. DURING AN ECHO-ENDOSCOPY, A NASO-JEJUNAL PROBE WAS PLACED. DURING THE INSTALLATION, IT WAS IMPOSSIBLE TO GET THE GUIDE OUT THROUGH THE END OF THE NASO-JEJUNAL PROBE. NO EXIT PORT. CONSEQUENCES WERE A LONGER EXAMINATION TIME AND A CHANGE OF DEVICE. THERE WAS NO HARM TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12217514 ↗
• MalfunctionJun 21, 2017Complete Blockage; Complete Blockage

  THE CUSTOMER REPORTS THAT IMMEDIATELY AFTER OPENING, THEY NOTICED THE HOLE IN THE TIP WAS CLOGGED THEREFORE CATHETER INSERTION WAS IMPOSSIBLE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6657965 ↗