FDA Adverse Event Injury Summary report: N

BARD ACCESS SYSTEMS

MDR report key: 455446 · Received March 31, 2003

Report

Report Number
455446
Event Type
Injury
Date Received
March 31, 2003
Date of Event
March 26, 2003
Report Date
March 31, 2003
Manufacturer
*
Product Code
DYB
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
FL, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PT HAD PICC INSERTED-GUIDEWIRE SLIPPED THROUGH INTRODUCER INTO ARM. PT HAD TO BE TRANSPORTED TO ANOTHER HOSPITAL TO RETREIVE GUIDEWIRE THROUGH FEMORAL ARTERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BARD ACCESS SYSTEMS UNIVERSAL MICROINTRODUCER KIT DYB * * 22AN2559

Patients

Seq Age Sex Outcome Treatment
1 72 YR Required Intervention