FDA Adverse Event Other Summary report: N

VITAL-PORT

MDR report key: 253250 · Received December 3, 1999

Report

Report Number
2522007-1999-00028
Event Type
Other
Date Received
December 3, 1999
Date of Event
December 17, 1999
Manufacturer
COOK VASCULAR, INC.
Product Code
LJT
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

AS REPORTED TO THE DISTRIBUTOR BY THE PHYSICIAN, THE VITAL-PORT HAD A LEAKAGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VITAL-PORT Implant VASCULAR ACCESS SYSTEM LJT COOK VASCULAR, INC. 7129 NA

Patients

Seq Age Sex Outcome Treatment
1 3 YR Other| R