FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS (50)

MDR report key: 1052390 · Received May 23, 2008

Report

Report Number
1826988-2008-00545
Event Type
Malfunction
Date Received
May 23, 2008
Date of Event
April 26, 2008
Report Date
April 26, 2008
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER STATED THAT SHE PERFORMED A CONTROL TEST AND REC'D A RESULT OF 298 MG/DL. WHILE TROUBLESHOOTING, SHE PERFORMED MORE CONTROL TESTS AND REC'D A RESULT OF 282 MG/DL. THE NORMAL CONTROL 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 METER NBW BAYER HEALTHCARE, LLC 7080D 7JC3B06

Patients

Seq Age Sex Outcome Treatment
1 UNK