FDA Adverse Event Injury Summary report: N

V12 COVERED STENT

MDR report key: 3121781 · Received May 15, 2013

Report

Report Number
1219977-2013-00058
Event Type
Injury
Date Received
May 15, 2013
Date of Event
March 22, 2013
Report Date
April 19, 2013
Manufacturer
ATRIUM MEDICAL CORPORATION
Product Code
JCT
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

AWAITING ADD'L DETAILS ON THE EVENT IN ORDER TO COMPLETE THE ANALYSIS. HOSPITAL DID PROVIDE A FILM FOR THE INVESTIGATION.

Description of Event or Problem · 1

HOSPITAL REPORTED THAT THE ADVANTA STENT GRAFT RUPTURED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
214704 V12 COVERED STENT PTFE COVERED STENT JCT ATRIUM MEDICAL CORPORATION 85353 10859002

Patients

Seq Age Sex Outcome Treatment
1 Other