ANEURX
Report
- Report Number
- 2953200-2014-02271
- Event Type
- Injury
- Date Received
- November 3, 2014
- Date of Event
- October 23, 2014
- Report Date
- May 5, 2015
- Manufacturer
- MEDTRONIC CARDIOVASCULAR
- Product Code
- MIH
- PMA / PMN Number
- P990020
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4).
ADDITIONAL INFORMATION WAS RECEIVED. PER THE PHYSICIAN, THE CAUSE OF THE PROXIMAL TYPE I ENDOLEAK WAS DUE TO DISEASE PROGRESSION.
AN ANEURX STENT GRAFT SYSTEM WAS IMPLANTED FOR THE ENDOVASCULAR TREATMENT OF A 6.7CM DIAMETER ABDOMINAL AORTIC ANEURYSM. CURRENTLY, THE PROXIMAL AORTIC NECK MEASURE 19MM IN DIAMETER AND IS ANGULATED 35 DEGREES. IT WAS REPORTED THAT ON A ROUTINE FOLLOW UP CT SCAN, IT WAS OBSERVED THAT THE BIFURCATE HAD MIGRATED. A PROXIMAL TYPE I ENDOLEAK WAS PRESENT. THE PHYSICIAN STATED THAT THE CAUSE OF THE EVENT WAS DUE TO DISEASE PROGRESSION. AN INTERVENTION WAS PERFORMED AND AN ENDURANT AUI LIMB AND TALENT OCCLUDER WERE IMPLANTED HOWEVER, A PROXIMAL TYPE I ENDOLEAK REMAINED. THE PHYSICIAN CHOOSE TO TREAT THE PROXIMAL TYPE I ENDOLEAK WITH AN APTUS DEVICE HOWEVER, THE TYPE I ENDOLEAK DID NOT RESOLVE. THE PHYSICIAN STATED THAT THE ENDOLEAK WOULD THROMBUS OFF AND NO FURTHER TREATMENT WOULD BE PLANNED AND NO FURTHER IMAGING IS SCHEDULED. NO ADDITIONAL CLINICAL SEQUELAE WERE REPORTED AND THE PATIENT IS FINE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 702361 | ANEURX | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | MIH | MEDTRONIC CARDIOVASCULAR | M03L550129 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00085 YR | Required Intervention |