FDA Adverse Event Summary report: N

BD VACUTAINER SAFETY-LOK BLOOD COLLECTION SET

MDR report key: 3973304 · Received June 23, 2014

Report

Report Number
3973304
Date Received
June 23, 2014
Date of Event
June 22, 2014
Report Date
June 23, 2014
Manufacturer
BECTON, DICKINSON AND COMPANY
Product Code
JKA
Report Source
User Facility report
Reporter Location
LA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

SAFETY COVER OF NEEDLE OF BLOOD COLLECTION SET WAS LOOSE IN PACKAGE AND NEEDLE WAS EXPOSED. NEEDLE COULD EASILY PIERCE THROUGH PACKAGING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
365768 BD VACUTAINER SAFETY-LOK BLOOD COLLECTION SET TUBES, VIALS, SYSTEMS, SERUM SEPARATORS, BLOOD COLLECTION JKA BECTON, DICKINSON AND COMPANY 23G X 3/4" X 12" 3325806

Patients

Seq Age Sex Outcome Treatment
1 *