FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS (50)

MDR report key: 1032099 · Received April 18, 2008

Report

Report Number
1826988-2008-00471
Event Type
Malfunction
Date Received
April 18, 2008
Date of Event
April 10, 2008
Report Date
April 10, 2008
Manufacturer
BAYER HEALTHCARE, LLC
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER ALLEGED THAT HE PERFORMED CONTROL TESTS AND REC'D RESULTS OF 413, 373, AND 381 MG/DL. THE NORMAL CONTROL RANGE WAS 99-136 MG/DL. NO ADVERSE EVENTS WERE ALLEGED. THE CUSTOMER DISPOSED OF THE CONTROL TEST SOLUTION, SO FURTHER TROUBLESHOOTING WAS NOT POSSIBLE. 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 NOT PROVIDED 6LC3C09

Patients

Seq Age Sex Outcome Treatment
1 UNK