FDA Adverse Event Malfunction Summary report: N

CONTOUR TEST STRIPS

MDR report key: 1854419 · Received September 29, 2010

Report

Report Number
1826988-2010-00679
Event Type
Malfunction
Date Received
September 29, 2010
Date of Event
September 21, 2010
Report Date
September 21, 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
NJ, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

THE CUSTOMER CALLED FOR HELP WITH HER CONTOUR METER. SHE PERFORMED CONTROL TESTS AND REC'D RESULTS OF 555, 512 AND 286 MG/DL. THE NORMAL CONTROL RANGE WAS 107-148 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 7070A 9JC3B31

Patients

Seq Age Sex Outcome Treatment
1 UNK