FDA Adverse Event Malfunction Summary report: N

CONTOUR

MDR report key: 2874448 · Received December 14, 2012

Report

Report Number
1826988-2012-00658
Event Type
Malfunction
Date Received
December 14, 2012
Date of Event
November 1, 2012
Report Date
November 28, 2012
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 RAN HIS BLOOD GLUCOSE ON THE CONTOUR USB AND THE CONTOUR METERS. HE RECEIVED READINGS OF 64 AND 130MG/DL, RESPECTIVELY. THE DIFFERENCE BETWEEN THE READINGS FALLS IN THE "C" ZONE OF THE CONSENSUS ERROR GRID, MAKING THE DIFFERENCE CLINICALLY SIGNIFICANT. NO ADVERSE EVENTS WERE ALLEGED. THE TEST STRIPS ARE TO BE RETURNED FOR EVALUATION. REPLACEMENT TEST STRIPS AND A NEW METER WERE SENT TO THE CUSTOMER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONTOUR BLOOD GLUCOSE TEST STRIPS NBW BAYER HEALTHCARE LLC 7098C 2EC3F13

Patients

Seq Age Sex Outcome Treatment
1