FDA Adverse Event Malfunction Summary report: N

BD PARADIGM LINK GLUCOSE MONITOR

MDR report key: 1070371 · Received July 3, 2008

Report

Report Number
3004193489-2008-00494
Event Type
Malfunction
Date Received
July 3, 2008
Date of Event
June 21, 2008
Report Date
July 3, 2008
Manufacturer
NOVA BIOMEDICAL CORPORATION
Product Code
NBW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

NOVA BIOMEDICAL AWAITS THE RETURN OF THE DEVICE FOR EVAL. 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 SWITCHED UNITS OF MEASURE FROM MG/DL TO MMOL/DL. THE METER IN QUESTION WILL BE RETURNED FOR EVAL.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 UNK