FDA Adverse Event Malfunction Summary report: N

TRUEMETRIX

MDR report key: 6085710 · Received November 8, 2016

Report

Report Number
1000113657-2016-01839
Event Type
Malfunction
Date Received
November 8, 2016
Date of Event
October 18, 2016
Report Date
November 8, 2016
Manufacturer
TRIVIDIA HEALTH, INC.
Product Code
NBW
PMA / PMN Number
K140100
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). INVESTIGATION COMPLETED AND PRODUCT EVALUATED WITH NO DEFECT FOUND ON RETURNED METER. COSTUMER RETURNED NO SUFFICIENT TEST STRIPS (1) TO EVALUATE. MOST LIKELY UNDERLYING ROOT CAUSE OF MALFUNCTION: USER'S TEST STRIPS HAD A POOR STORAGE(KITCHEN).

Description of Event or Problem · 1

COSTUMER REPORTED COMPLAINT FOR HIGH BLOOD GLUCOSE TEST RESULTS. THE CUSTOMER IS CONCERNED WITH TEST RESULTS FROM RESULTS OBTAINED OF 162, 165 AND 146 MG/DL. THE CUSTOMER'S EXPECTED FASTING BLOOD GLUCOSE TEST RESULT RANGE IS 130 - 145 MG/DL. THE CUSTOMER FEELS WELL AND DID NOT REPORT ANY SYMPTOMS. MEDICAL ATTENTION IS NOT REPORTED AS A RESULT OF THE ACTUAL BLOOD GLUCOSE RESULTS. DURING THE CALL ON (B)(6) 2016, A BACK TO BACK BLOOD TEST WAS PERFORMED BY THE CUSTOMER FASTING AND PRODUCED TEST RESULTS OF 205 MG/DL AND 258 MG/DL. THE PRODUCT IS NOT STORED ACCORDING TO SPECIFICATION, CUSTOMER STORES THE PRODUCT IN THE KITCHEN. THE TEST STRIP LOT MANUFACTURER'S EXPIRATION DATE IS 08/31/2017 AND OPEN VIAL DATE IS (B)(6) 2016. THE METER MEMORY WAS REVIEWED FOR PREVIOUS TEST RESULT HISTORY:(TIME NOT SET CORRECTLY): (B)(4). CUSTOMER EDUCATED OF PRODUCT PROPER STORAGE ENVIRONMENTAL CONDITIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
738340 TRUEMETRIX BLOOD GLUCOSE SYSTEM NBW TRIVIDIA HEALTH, INC. TRUEMETRIX MT1660

Patients

Seq Age Sex Outcome Treatment
1 0 YR SECOND THERAPY