FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS

MDR report key: 1884659 · Received October 25, 2010

Report

Report Number
1826988-2010-00714
Event Type
Malfunction
Date Received
October 25, 2010
Date of Event
October 7, 2010
Report Date
October 7, 2010
Manufacturer
BAYER HEALTHCARE LLC
Product Code
NBW
PMA / PMN Number
K062058
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

THE ADVOCATE CALLED FOR HELP WITH THE CUSTOMER'S CONTOUR METER. WHILE TROUBLESHOOTING, HE PERFORMED CONTROL TESTS AND REC'D A RESULT OF 16 MG/DL. THE NORMAL CONTROL RANGE WAS 105-146 MG/DL. NO ADVERSE EVENTS WERE ALLEGED. THE TEST STRIPS ARE TO BE RETURNED FOR EVAL. REPLACEMENT TEST STRIPS AND A NEW METER WERE SENT TO THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONTOUR TEST STRIPS NBW BAYER HEALTHCARE LLC 7097C 9GC3C10

Patients

Seq Age Sex Outcome Treatment
1 UNK