FDA Adverse Event Injury Summary report: N

BARD ACCESS SYSTEMS

MDR report key: 1276143 · Received December 30, 2008

Report

Report Number
MW5009463
Event Type
Injury
Date Received
December 30, 2008
Date of Event
December 2, 2008
Report Date
December 30, 2008
Manufacturer
BARD ACCESS SYSTEMS INC.
Product Code
LJS
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MN, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT CAME TO ER BECAUSE PICC BROKE. PT PUT CLAMP FROM HOME IV INFUSION SET INTO TUBING. PICC SEPARATED JUST BELOW THE HUB. PT NOTED PROBLEM AFTER SHOWER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BARD ACCESS SYSTEMS CENTRAL VENOUS CATHETERS-SINGLE LUMEN BARD GROSHONG NT LJS BARD ACCESS SYSTEMS INC. 9617408 RESG0671

Patients

Seq Age Sex Outcome Treatment
1 49 YR Hospitalization