FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS

MDR report key: 1854361 · Received September 29, 2010

Report

Report Number
1826988-2010-00678
Event Type
Malfunction
Date Received
September 29, 2010
Date of Event
September 16, 2010
Report Date
September 16, 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
MN, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

THE ADVOCATE CALLED FOR HELP WITH THE CUSTOMER'S CONTOUR METER. SHE PERFORMED CONTROL TESTS DURING THE CALL AND RECEIVED A RESULT OF 51 MG/DL. THE NORMAL CONTROL RANGE WAS 111-153 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 9LC3D10

Patients

Seq Age Sex Outcome Treatment
1 UNK