FDA Adverse Event Injury Summary report: N

BD INSYTE AUTOGUARD

MDR report key: 518582 · Received March 25, 2004

Report

Report Number
MW4003658
Event Type
Injury
Date Received
March 25, 2004
Date of Event
February 9, 2004
Report Date
February 13, 2004
Manufacturer
BD MEDICAL SYSTEMS
Product Code
FOZ
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PT ADMITTED THRU ED FOR ASTHMA. STAFF NOTED BLEEDING & HUB OF CATHETER MISSING & WAS UNABLE TO RETRIEVE PINK CATHETER TIP FROM IV SITE. SURGEON TOOK TO O.R. FOR RETRIEVAL OF CATHETER TIP FROM VEIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BD INSYTE AUTOGUARD IV CATHETER FOZ BD MEDICAL SYSTEMS * *

Patients

Seq Age Sex Outcome Treatment
1 38 YR Required Intervention