FDA Adverse Event Injury Summary report: N

VAXCEL PERIPHERALLY INSERTED CENTRAL CATHETERS

MDR report key: 1202348 · Received October 13, 2008

Report

Report Number
MW5008654
Event Type
Injury
Date Received
October 13, 2008
Date of Event
October 2, 2008
Report Date
October 13, 2008
Manufacturer
BOSTON SCIENTIFIC
Product Code
LJS
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
IA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PICC LINE INSERTED AND WHITE CATHETER PORT LEAKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VAXCEL PERIPHERALLY INSERTED CENTRAL CATHETERS VAXCEL PICC LINE LJS BOSTON SCIENTIFIC PASV 5F 1284570

Patients

Seq Age Sex Outcome Treatment
1 Disability