FDA Adverse Event Malfunction Summary report: N

KANGAROO

MDR report key: 22196349 · Received June 12, 2025

Report

Report Number
1423537-2025-00245
Event Type
Malfunction
Date Received
June 12, 2025
Date of Event
February 18, 2025
Report Date
July 14, 2025
Manufacturer
CARDINAL HEALTH, INC.
Product Code
KNT
UDI-DI
10884521007291
PMA / PMN Number
K180622
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

ADDITIONAL 510 K NUMBER: K932295. ADDITIONAL PRODUCT CODE: PIF. AN INVESTIGATION IS CURRENTLY UNDERWAY. UPON COMPLETION, THE RESULTS WILL BE FORWARDED.

Additional Manufacturer Narrative · 0

THE DEVICE HISTORY RECORD REVIEW COULD NOT BE PERFORMED SINCE NO LOT NUMBER WAS PROVIDED. A SAMPLE WAS NOT RECEIVED FOR THE INVESTIGATION. BECAUSE A SAMPLE WAS NOT RETURNED, WE WERE UNABLE TO PERFORM A FOLLOW-UP INVESTIGATION TO INCLUDE FUNCTIONAL AND VISUAL EVALUATIONS TO CONFIRM THE ISSUE AND ROOT CAUSE ANALYSIS. HOWEVER, AS A PART OF CONTINUOUS IMPROVEMENTS, A SUPPLIER CORRECTIVE ACTION REQUEST (SCAR) HAS BEEN ISSUED TO THE SUPPLIER TO ADDRESS THE REPORTED CONDITION THROUGH A MORE ROBUST INVESTIGATION AND RESULTS OF THE INVESTIGATION WILL BE DOCUMENTED THROUGH THE REFERRED CAPA.

Description of Event or Problem · 0

THE CUSTOMER REPORTED THAT THE BROKEN BLADDER CAUSED INTERNALLY LEAKAGE. PER CUSTOMER, EVERYTHING WORKS NORMALLY UNTIL THE "BLADDER" BREAKS, FORCING THEM TO GET THE NURSE BACK TO CHANGE THE TUBE. THE PATIENT HAS A NURSE WHO PLACES THEM AND CHANGES THEM, AND SHE IS SPECIALIZED IN TUBE FEED. ADDITIONAL INFORMATION WAS RECEIVED FROM THE CUSTOMER AND STATED THAT "BLADDER BREAKS" REFERS TO BALLOON SPLITS/BREAKS. THERE WAS NO HARM REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1362106 KANGAROO TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT CARDINAL HEALTH, INC. 8884720205 10884521007291

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown