FDA Adverse Event Injury Summary report: N

ARTERIOVENOUS GRAFT

MDR report key: 11826 · Received March 1, 1994

Report

Report Number
MW1000945
Event Type
Injury
Date Received
March 1, 1994
Date of Event
January 4, 1993
Report Date
February 1, 1994
Manufacturer
UNKNOWN
Product Code
FIQ
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT HAD EXCISION OF LEFT ARM VEIN AND ARTERIOVENOUS GRAFT FROM LEFT ARM FOR THROMBOSIS/ACUTE INFLAMMATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ARTERIOVENOUS GRAFT Implant FIQ UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 80 YR Required Intervention