FDA Adverse Event Summary report: N

MULTI-LINK MINI VISION

MDR report key: 1032571 · Received March 27, 2008

Report

Report Number
1032571
Date Received
March 27, 2008
Date of Event
March 13, 2008
Report Date
March 20, 2008
Manufacturer
ABBOTT VASCULAR DEVICES
Product Code
MAF
Report Source
User Facility report
Reporter Location
AL, US

Narratives

Description of Event or Problem · 1

A STENT CAME OFF OF THE BALLOON AND WAS LOST.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MULTI-LINK MINI VISION STENT, CORONARY MAF ABBOTT VASCULAR DEVICES * 8020631

Patients

Seq Age Sex Outcome Treatment
1 35 YR