| Brand Name | Kangaroo |
| Common Device Name | Tubes, Gastrointestinal (And Accessories) |
| Manufacturer (Section D) |
| Cardinal Health, Inc. |
| 3651 birchwood drive |
| waukegan IL 60085 |
|
| Manufacturer (Section G) |
| Cardinal Health |
| calle 9 sur no. 125 cuidad ind |
|
| tijuana 22500 |
|
MX
22500
|
|
| Manufacturer Contact |
|
jill
saraiva
|
| 3651 birchwood drive |
| waukegan, IL 60085
|
|
+1(508)618-3640
|
|
| MDR Report Key | 50821835 |
| Report Number | 1423537-2026-00298 |
| Device Sequence Number | 10218798 |
| Product Code |
KNT
|
| UDI-Device Identifier | 10884521582897 |
| UDI-Public | (01)10884521582897(17)280229(10)2306615264 |
| Combination Product (Y/N) | N |
| Initial Reporter State | CO |
| Initial Reporter Country | US |
| PMA/510(K) Number | K112511 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
User Facility,Company Representative |
| Type of Report
| Initial |
| Report Date (Section B) |
09/18/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
No
|
| Is this a Product Problem Report? |
Yes
|
| Operator of Device |
Health Professional
|
| Device Model Number | 8884710867E |
| Device Catalogue Number | 8884710867E |
| Device Lot Number | 2306615264 |
| Was Device Available for Evaluation? |
Yes
|
| Is the Reporter a Health Professional? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 09/08/2026 |
| Initial Report FDA Received Date | 09/18/2026 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |