FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS (50)

MDR report key: 1212738 · Received October 20, 2008

Report

Report Number
1826988-2008-01188
Event Type
Malfunction
Date Received
October 20, 2008
Date of Event
September 30, 2008
Report Date
September 30, 2008
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE ADVOCATE CALLED FOR HELP WITH THE CUSTOMER'S METER. WHILE TROUBLESHOOTING, THE ADVOCATE PERFORMED CONTROL TESTS AND RECEIVED A RESULT OF 45 MG/DL. THE NORMAL CONTROL RANGE WAS 105-145 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 7098B 8BC3B03

Patients

Seq Age Sex Outcome Treatment
1 UNK