FDA Adverse Event
Death
Summary report: N
MEDTRONIC VALIANT STENT
MDR report key: 18989995
·
Received March 27, 2024
Report
- Report Number
- MW5153273
- Event Type
- Death
- Date Received
- March 27, 2024
- Report Date
- March 27, 2024
- Manufacturer
- MEDTRONIC IRELAND
- Product Code
- MIH
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- UNKNOWN
- Health Professional
- *
Narratives
Description of Event or Problem · 0
THIS CONSUMER COMPLAINT WAS REGARDING A DEATH AFTER AN IMPLANT OF MEDTRONIC VALIANT STENTS. THE COMPLAINANT LIVES IN CHINA AND STENTS WERE MANUFACTURED IN IRELAND. REFERENCE REPORT: MW5153272.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 721343 | MEDTRONIC VALIANT STENT | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | MIH | MEDTRONIC IRELAND |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Death |