FDA Adverse Event Other Summary report: N

SAF-T-INTIMA IV CATHETER

MDR report key: 546898 · Received September 29, 2004

Report

Report Number
9610847-2004-00011
Event Type
Other
Date Received
September 29, 2004
Report Date
August 26, 2004
Manufacturer
BECTON DICKINSON INFUSION THERAPY SYSTEMS
Product Code
DQO
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

SAF-T-INTIMA HAS CAUSED A NEEDLESTICK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SAF-T-INTIMA IV CATHETER INTRAVASCULAR CATHETERS DQO BECTON DICKINSON INFUSION THERAPY SYSTEMS NA UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other