FDA Adverse Event Malfunction Summary report: N

BBL VACUTAINER

MDR report key: 2862304 · Received December 3, 2012

Report

Report Number
2862304
Event Type
Malfunction
Date Received
December 3, 2012
Date of Event
November 30, 2012
Report Date
December 3, 2012
Manufacturer
BECTON DICKINSON
Product Code
JTX
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CO, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

THREE OF THE ANAEROBIC SPECIMEN TUBES BROKE DURING NORMAL USE. ALSO, IT APPEARED THERE WAS MOISTURE INSIDE THE TUBES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BBL VACUTAINER TRANSPORT SYSTEMS, ANAEROBIC JTX BECTON DICKINSON * 2061411
2 BBL VACUTAINER TRANSPORT SYSTEMS, ANAEROBIC JTX BECTON DICKINSON * 2146020
3 BBL VACUTAINER TRANSPORT SYSTEMS, ANAEROBIC JTX BECTON DICKINSON * 1242294

Patients

Seq Age Sex Outcome Treatment
1 *