FDA Adverse Event Malfunction Summary report: N

6913744

MDR report key: 6913744 · Received October 4, 2017

Report

Report Number
6913744
Event Type
Malfunction
Date Received
October 4, 2017
Date of Event
August 28, 2017
Report Date
September 25, 2017
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PHLEBOTOMIST WAS DRAWING PATIENT'S BLOOD WHEN THE NEEDLE STARTED TO COME LOOSE FROM THE HOLDER. PHLEBOTOMIST MANAGED TO SCREW HOLDER BACK ONTO THE NEEDLE WITHOUT HARM TO PATIENT.

Patients

Seq Age Sex Outcome Treatment
1 Other NO| NO OTHER THERAPIES