FDA Adverse Event Malfunction Summary report: N

CONTOUR

MDR report key: 3090419 · Received May 2, 2013

Report

Report Number
1826988-2013-00184
Event Type
Malfunction
Date Received
May 2, 2013
Date of Event
April 1, 2013
Report Date
April 8, 2013
Manufacturer
BAYER HEALTHCARE LLC
Product Code
NBW
PMA / PMN Number
K062058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER RECEIVED A BLOOD GLUCOSE READING OF 135MG/DL ON THE CONTOUR METER, RE-TESTED ON THE CONTOUR USB METER AND THE READING WAS 348MG/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 TEST STRIPS ARE NOT AVAILABLE TO RETURN FOR EVALUATION. A NEW METER WAS SENT TO THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
192434 CONTOUR BLOOD GLUCOSE METER NBW BAYER HEALTHCARE LLC 9556C

Patients

Seq Age Sex Outcome Treatment
1