FDA Adverse Event Other Summary report: N

SIM'S PORTEX ABG SYRINGE, NEEDLE-PRO

MDR report key: 389423 · Received April 19, 2002

Report

Report Number
389423
Event Type
Other
Date Received
April 19, 2002
Date of Event
February 10, 2002
Report Date
April 4, 2002
Manufacturer
SIMS PORTEX, INC.
Product Code
GJE
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
OR, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

AFTER DRAWING ARTERIAL BLOOD GASES, NURSE ATTEMPTED TO COVER NEEDLE WITH THE NEEDLE PROTECTOR. INITIALLY THE PROTECTOR DID NOT ENGAGE-NURSE USED MORE FORCE AND THOUGHT PROTECTOR HAD ENGAGED. AS NURSE ATTEMPTED TO REMOVE THE NEEDLE, NEEDLE WAS NOT PROTECTED AND NURSE SUSTAINED NEEDLE STICK TO RIGHT MIDDLE FINGER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SIM'S PORTEX ABG SYRINGE, NEEDLE-PRO ABG SYRINGE GJE SIMS PORTEX, INC. * K101563 OR K101571

Patients

Seq Age Sex Outcome Treatment
1 36 YR Other