FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS

MDR report key: 2212074 · Received July 8, 2011

Report

Report Number
1826988-2011-00398
Event Type
Malfunction
Date Received
July 8, 2011
Date of Event
June 1, 2011
Report Date
June 20, 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
ID, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER TESTED HIS BLOOD GLUCOSE USING HIS CONTOUR METER AND RECEIVED A READING OF 54 MG/DL. HE RETESTED USING ANOTHER METER AND RECEIVED A READING OF 181 MG/DL. 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 TEST STRIPS NBW BAYER HEALTHCARE LLC 7080G 1BC3C09

Patients

Seq Age Sex Outcome Treatment
1 UNK