FDA Adverse Event Malfunction Summary report: N

CONTOUR

MDR report key: 3090306 · Received May 2, 2013

Report

Report Number
1826988-2013-00180
Event Type
Malfunction
Date Received
May 2, 2013
Date of Event
April 3, 2013
Report Date
April 3, 2013
Manufacturer
BAYER HEALTHCARE LLC
Product Code
NBW
PMA / PMN Number
K062058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER RECEIVED A BLOOD GLUCOSE READING OF HI ON THE CONTOUR METER, RE-TESTED ON A DIFFERENT METER AND THE READING WAS 128MG/DL. THE DIFFERENCE BETWEEN THE READINGS FALLS IN THE "C" ZONE OF THE CONSENSUS ERROR GRID, MAKING THE DIFFERENCE CLINICALLY SIGNIFICANT NO ADVERSE EVENT WAS ALLEGED. THE CUSTOMER WAS ADVISED TO RETURN THE TEST STRIPS FOR EVALUATION. REPLACEMENT TEST STRIPS AND METER WERE SENT TO THE CUSTOMER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
191518 CONTOUR BLOOD GLUCOSE TEST STRIPS NBW BAYER HEALTHCARE LLC 7080G 2KC3D04

Patients

Seq Age Sex Outcome Treatment
1