FDA Adverse Event Malfunction Summary report: N

BD LOGIC BLOOD GLUCOSE MONITOR

MDR report key: 1040796 · Received May 9, 2008

Report

Report Number
3004193489-2008-00399
Event Type
Malfunction
Date Received
May 9, 2008
Date of Event
April 23, 2008
Report Date
May 9, 2008
Manufacturer
NOVA BIOMEDICAL CORPORATION
Product Code
NBW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

NOVA BIOMEDICAL AWAITS THE RETURN OF THE DEVICE FOR EVALUATION. SHOULD ANY SIGNIFICANT FINDINGS BE A RESULT OF THAT INVESTIGATION, A FOLLOW-UP REPORT WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED TO NOVA BIOMEDICAL THAT A CONSUMER'S BLOOD GLUCOSE METER WAS MISSING THE LAST DIGIT IN THE LCD RESULTS SCREEN. THE METER IN QUESTION WILL BE RETURNED FOR EVALUATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BD LOGIC BLOOD GLUCOSE MONITOR GLUCOSE MONITOR NBW NOVA BIOMEDICAL CORPORATION NA NA

Patients

Seq Age Sex Outcome Treatment
1 UNK