FDA Adverse Event Malfunction Summary report: N

PICC LINE

MDR report key: 1132863 · Received August 14, 2008

Report

Report Number
MW5008064
Event Type
Malfunction
Date Received
August 14, 2008
Date of Event
July 16, 2008
Report Date
July 16, 2008
Manufacturer
BOSTON SCIENTIFIC CORP.
Product Code
LJS
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OH, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PREPARING PICC LINE FOR INSERTION. UNABLE TO FLUSH RED PORT. DEVICE NOT USED ON A PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PICC LINE LJS BOSTON SCIENTIFIC CORP. 1271232

Patients

Seq Age Sex Outcome Treatment
1 NA Other