FDA Adverse Event Malfunction Summary report: N

CONTOUR TS TEST STRIPS

MDR report key: 2222370 · Received July 15, 2011

Report

Report Number
1826988-2011-00403
Event Type
Malfunction
Date Received
July 15, 2011
Date of Event
June 21, 2011
Report Date
June 21, 2011
Manufacturer
BAYER HEALTHCARE LLC
Product Code
NBW
PMA / PMN Number
K062058
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER CALLED FOR HELP WITH HIS CONTOUR TS METER. HE PERFORMED CONTROL TESTS DURING THE CALL AND REC'D A RESULT OF 24 AND 42 MG/DL. THE NORMAL CONTROL RANGE WAS 100-138 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 TS TEST STRIPS NBW BAYER HEALTHCARE LLC 1820 0AD3E04

Patients

Seq Age Sex Outcome Treatment
1 UNK