FDA Adverse Event Death Summary report: N

BACTEC PEDS PLUS/F MEDIUM

MDR report key: 161020 · Received April 4, 1998

Report

Report Number
1119779-1998-00004
Event Type
Death
Date Received
April 4, 1998
Report Date
March 2, 1998
Manufacturer
BECTON DICKINSON MICROBIOLOGY SYSTEMS
Product Code
JTA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PT SPECIMEN WAS NOT FLAGGED AS POSITIVE DURING TESTING OF PEDS PLUS VIAL. VIAL WAS SUBCULTURED AS STREP PNEUMO. THE PT EXPIRED SOMETIME AFTER THE SPECIMEN WAS DRAWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BACTEC PEDS PLUS/F MEDIUM CULTURE MEDIA JTA BECTON DICKINSON MICROBIOLOGY SYSTEMS NA 5127N

Patients

Seq Age Sex Outcome Treatment
1 34 YR Death