FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS

MDR report key: 1982540 · Received January 11, 2011

Report

Report Number
1826988-2010-00866
Event Type
Malfunction
Date Received
January 11, 2011
Date of Event
December 1, 2010
Report Date
December 16, 2010
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
PMA / PMN Number
K062058
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER TESTED HER BLOOD GLUCOSE USING HER 2 CONTOUR METERS AND RECEIVED READINGS OF 62 AND 129 MG/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 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 TEST STRIPS NBW BAYER HEALTHCARE, LLC 7080G 0EC3C05

Patients

Seq Age Sex Outcome Treatment
1 UNK