FDA Adverse Event Other Summary report: N

SST BRAND TUBE-16X100MM, 8.3ML, RED/GRAY CONVENTIONAL TUBE

MDR report key: 297054 · Received September 21, 2000

Report

Report Number
1024879-2000-00021
Event Type
Other
Date Received
September 21, 2000
Date of Event
August 30, 2000
Report Date
September 21, 2000
Manufacturer
BECTON DICKINSON & CO.
Product Code
JKA
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PHLEBOTOMIST RECEIVED A CUT FROM A BROKEN GLASS TUBE WHICH REQUIRED FIRST AID. BASELINE TESTING CONSISTED OF HIV AND HEPATITIS B & C. FOLLOW UP TESTING TO BE PERFORMED AT QUEST'S APPROPRIATE INTERNAL. ACCOUNT FEELS NO DEGREE OF RISK BASED ON SOURCE OF EXPOSURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SST BRAND TUBE-16X100MM, 8.3ML, RED/GRAY CONVENTIONAL TUBE SST TUBE JKA BECTON DICKINSON & CO. NA 0D928

Patients

Seq Age Sex Outcome Treatment
1 NA Other