FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPD

MDR report key: 2222366 · Received July 15, 2011

Report

Report Number
1826988-2011-00408
Event Type
Malfunction
Date Received
July 15, 2011
Date of Event
June 1, 2011
Report Date
June 23, 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
NE, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER TESTED HIS BLOOD GLUCOSE USING HIS 2 CONTOUR METERS AND REC'D READINGS OF 45 AND 75 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 TEST STRIPS ARE TO BE RETURNED FOR EVAL. REPLACEMENT TEST STRIPS WERE SENT TO THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONTOUR TEST STRIPD NBW BAYER HEALTHCARE LLC 7080G 0GC3D03

Patients

Seq Age Sex Outcome Treatment
1 UNK