FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS (50)

MDR report key: 1271698 · Received November 26, 2008

Report

Report Number
1826988-2008-01417
Event Type
Malfunction
Date Received
November 26, 2008
Date of Event
November 18, 2008
Report Date
November 18, 2008
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US

Narratives

Description of Event or Problem · 1

THE CUSTOMER CALLED FOR HELP WITH HER NEW METER. SHE PERFORMED CONTROL TESTS AND RECEIVED A RESULT OF 60 MG/DL. THE NORMAL CONTROL RANGE WAS 103-142 MG/DL. NO ADVERSE EVENTS WERE ALLEGED. THE TEST STRIPS ARE TO BE RETURNED FOR EVALUATION. REPLACEMENT TEST STRIPS WERE SENT TO THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONTOUR TEST STRIPS (50) BLOOD GLUCOSE TEST STRIPS NBW BAYER HEALTHCARE, LLC 7080G 8CC3A05

Patients

Seq Age Sex Outcome Treatment
1 UNK