FDA Adverse Event Death Summary report: N

MEDI. TECH BOSTON SCIENTIFIC CORP.

MDR report key: 207862 · Received January 26, 1999

Report

Report Number
207862
Event Type
Death
Date Received
January 26, 1999
Date of Event
January 24, 1999
Report Date
January 25, 1999
Manufacturer
MEDITECH BOSTON SCIENTIFIC CORP
Product Code
DTK
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PT TO OPERATING ROOM FOR GREENFIELD VENA CAVA UMBRELLA. VENA CAVAL PERFORATION WHEN UMBRELLA DEPLOYED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDI. TECH BOSTON SCIENTIFIC CORP. Implant TITANIUM GREENFIELD VENA CAVA FILTER DTK MEDITECH BOSTON SCIENTIFIC CORP * 275772

Patients

Seq Age Sex Outcome Treatment
1 86 YR Death