FDA Adverse Event
Injury
Summary report: N
KANGAROO
MDR report key: 24788648
·
Received April 6, 2026
Report
- Report Number
- 1423537-2026-00099
- Event Type
- Injury
- Date Received
- April 6, 2026
- Report Date
- May 4, 2026
- Manufacturer
- CARDINAL HEALTH 200, LLC
- Product Code
- KNT
- UDI-DI
- 10192253007831
- PMA / PMN Number
- K163002
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WI, US
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
Additional Manufacturer Narrative · 0
ADDITIONAL PRODUCT CODE: PIF. ADDITIONAL 510K NUMBER: K123555. AN INVESTIGATION IS CURRENTLY UNDERWAY. UPON COMPLETION THE RESULTS WILL BE FORWARDED.
Description of Event or Problem · 0
THE CUSTOMER REPORTED THE PATIENT HAD A VAGUS NERVE STIMULATOR. AN INSERTER REPORTED A PATIENT HAVING A SEIZURE AFTER PLACING AN IRIS TUBE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 600566 | KANGAROO | TUBES, GASTROINTESTINAL (AND ACCESSORIES) | KNT | CARDINAL HEALTH 200, LLC | 461043E | 1055070825 | 10192253007831 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |