ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
Report
- Report Number
- 1820334-2013-00293
- Event Type
- Injury
- Date Received
- July 12, 2013
- Date of Event
- June 6, 2013
- Report Date
- July 1, 2013
- Manufacturer
- COOK, INC.
- Product Code
- MIH
- PMA / PMN Number
- P020018
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). EVENT EVAL: STILL UNDER INVESTIGATION.
INFO FROM A STUDY INDICATES THAT A (B)(6) MALE UNDERWENT EVAR ON (B)(6) 2013. THE PHYSICIAN PLACED ZENITH ENDOGRAFTS INCLUDING ILIAC LIMBS WITH SPIRAL-Z TECHNOLOGY. THE PATIENT HAD MODERATE LEFT ILIAC DISEASE AND CALCIFICATION WITH MILD LEFT ILIAC TORTUOSITY. THE RIGHT HAD MODERATE ILIAC OCCLUSIVE DISEASE AND CALCIFICATION WITH NO RIGHT ILIAC TORTUOSITY. AT THE END OF THE PROCEDURE, IT WAS NOTED THAT THERE WAS A PROXIMAL TYPE I ENDOLEAK THAT HAD NOT BEEN RESOLVED BY THE END OF THE PROCEDURE. AS OF (B)(6) 2013, IT WAS NOTED THAT BOTH THE LEFT AND RIGHT ILIACS HAD EXTERNAL COMPRESSION. HOWEVER, AT THIS TIME IT IS UNK IF ANY ADD'L DEVICES WERE PLACED AS IT WAS NOT PROVIDED BY THE REPORTER. ADD'L QUESTIONS HAVE BEEN ASKED BUT INFO HAS NOT YET BEEN PROVIDED. ADD'L INFO RECEIVED ON (B)(4) 2013 FROM THE STUDY INDICATED THAT THERE WAS A RIGHT AND LEFT ANGIOPLASTY PERFORMED IN THE LEG/LEG EXTENSION AFTER THE PROCEDURE DUE TO EXTERNAL COMPRESSION ON BOTH SIDES (1820334-2013-00292). THERE WAS NO EXTERNAL COMPRESSION OBSERVED AT THE CONCLUSION OF THE PROCEDURE. THE TYPE I ENDOLEAK WAS A PROXIMAL ENDOLEAK (1820334-2013-00293). ALL ZENITH DEVICES REMAIN IMPLANTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 321706 | ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY | MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | MIH | COOK, INC. | NA | 4101269 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Required Intervention |