FDA Adverse Event Malfunction Summary report: N

CONTOUR TS TEST STRIPS (50)

MDR report key: 1024229 · Received March 27, 2008

Report

Report Number
1826988-2008-00310
Event Type
Malfunction
Date Received
March 27, 2008
Date of Event
February 29, 2008
Report Date
February 29, 2008
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER STATED THAT HE TESTED HIS BLOOD GLUCOSE AND RECEIVED A READING OF 311 MG/DL USING HIS CONTOUR METER. HE RETESTED USING ANOTHER METER AND RECEIVED A READING OF 140 MG/DL. THE DIFFERENCE BETWEEN THE READINGS FALLS IN THE "C" ZONE OF THE PARKES ERROR GRID, MAKING THE DIFFERENCE CLINICALLY SIGNIFICANT. NO ADVERSE EVENTS WERE 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 TS TEST STRIPS (50) BLOOD GLUCOSE TEST STRIPS NBW BAYER HEALTHCARE, LLC 1820 7KD3E01

Patients

Seq Age Sex Outcome Treatment
1 UNK