FDA Adverse Event Malfunction Summary report: N

BD PARADIGM LINK GLUCOSE MONITOR

MDR report key: 1031443 · Received April 18, 2008

Report

Report Number
3004193489-2008-00389
Event Type
Malfunction
Date Received
April 18, 2008
Date of Event
April 15, 2008
Report Date
April 18, 2008
Manufacturer
NOVA BIOMEDICAL CORPORATION
Product Code
NBW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

NOVA MEDICAL 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 RECEIVED A RESULT OF "LO" (LESS THAN 20 MG/DL) ON THEIR BLOOD GLUCOSE METER. THE CONSUMER IMMEDIATELY PERFORMED AN ADDITIONAL FIVE TESTS USING THE SAME METER AND STRIPS GETTING THE FOLLOWING RESULTS OF 152 MG/DL, "LO", "LO", 141 MG/DL, 124 MG/DL. THE DIFFERENCE IN THE READINGS WAS DETERMINED TO BE CLINICALLY SIGNIFICANT. THE TEST STRIPS 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 1020207219

Patients

Seq Age Sex Outcome Treatment
1 UNK