FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS (50)

MDR report key: 1157543 · Received September 2, 2008

Report

Report Number
1826988-2008-00933
Event Type
Malfunction
Date Received
September 2, 2008
Date of Event
August 1, 2008
Report Date
August 1, 2008
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER STATED THAT THE CUSTOMER PERFORMED CONTROL TESTS AND REC'D RESULTS OF 189 AND 186 MG/DL. THE NORMAL RANGE WAS 103-142 MG/DL. 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 TEST STRIPS (50) BLOOD GLUCOSE TEST STRIPS NBW BAYER HEALTHCARE, LLC 7080G 8CC3A05

Patients

Seq Age Sex Outcome Treatment
1 UNK