FDA Adverse Event Other Summary report: N

BARD 4 FR SINGLE LUMEN POWERPICC

MDR report key: 3434285 · Received October 24, 2013

Report

Report Number
MW5032401
Event Type
Other
Date Received
October 24, 2013
Date of Event
October 7, 2013
Report Date
October 11, 2013
Manufacturer
BARD ACCESS SYSTEMS, INC.
Product Code
LJS
Report Source
Voluntary report
Reporter Location
CO, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PATIENT HAD PICC INSERTED ON OR SHORTLY BEFORE (B)(6) 2013. PATIENT REFERRED TO RADIOLOGIST/CATH LAB FOR REMOVAL ON (B)(6) 2013, DUE TO KNOT IN PICC APPROX 2 CM FROM END. DOCTOR OFFICE UNABLE TO REMOVE IT. PICC REMOVED THROUGH IJ ACCESS USING SNARE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
546344 BARD 4 FR SINGLE LUMEN POWERPICC PICC LINE LJS BARD ACCESS SYSTEMS, INC. REXG0322

Patients

Seq Age Sex Outcome Treatment
1 50 YR