FDA Adverse Event Malfunction Summary report: N

CONTOUR TS TEST STRIPS

MDR report key: 2223347 · Received August 16, 2011

Report

Report Number
1826988-2011-00471
Event Type
Malfunction
Date Received
August 16, 2011
Date of Event
July 1, 2011
Report Date
July 25, 2011
Manufacturer
BAYER HEALTHCARE LLC
Product Code
NBW
PMA / PMN Number
K062058
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER TESTED HER BLOOD GLUCOSE AND RECEIVED A READING OF 11 MG/DL FROM HER CONTOUR METER AND A READING OF 84 MG/DL FROM HER CONTOUR TS METER. 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 TO BE RETURNED FOR EVAL. 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 TS TEST STRIPS NBW BAYER HEALTHCARE LLC I820 0KD3D03

Patients

Seq Age Sex Outcome Treatment
1 UNK