FDA Adverse Event Malfunction Summary report: N

METRIX AIR

MDR report key: 6369172 · Received March 1, 2017

Report

Report Number
1000113657-2017-00411
Event Type
Malfunction
Date Received
March 1, 2017
Date of Event
February 4, 2017
Report Date
March 1, 2017
Manufacturer
TRIVIDIA HEALTH, INC.
Product Code
NBW
UDI-DI
00021292007447
PMA / PMN Number
K150052
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). PRODUCT NOT YET RETURNED FOR EVALUATION. MOST LIKELY UNDERLYING ROOT CAUSE OF MALFUNCTION: USER'S TEST STRIP HAD POOR STORAGE (BATHROOM). (B)(4).

Description of Event or Problem · 1

CONSUMER REPORTED COMPLAINT FOR HIGH BLOOD GLUCOSE TEST RESULTS. THE CUSTOMER IS CONCERNED WITH TESTS RESULTS FROM RESULTS OBTAINED OF 240, 269 AND 259 MG/DL. THE CUSTOMER'S EXPECTED FASTING BLOOD GLUCOSE TEST RESULT RANGE IS 115 - 130 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) 2017, A BACK TO BACK BLOOD TEST WAS NOT PERFORMED BY THE CUSTOMER. THE PRODUCT IS NOT STORED ACCORDING TO SPECIFICATION AND IS STORED IN THE BATHROOM. THE TEST STRIP LOT MANUFACTURER'S EXPIRATION DATE IS 03/24/2018 AND OPEN VIAL DATE IS 02/03/2017. THE CUSTOMER STATED HE HAS NOT HAD ANY RECENT CHANGES IN DIET, EXERCISE, OR MEDICATIONS. THE CUSTOMER STATED HE TAKES INSULIN FOR DIABETES MANAGEMENT BUT IS UNCERTAIN OF THE EXACT NAME. THE CUSTOMER PROVIDED THE LAST FIVE RESULTS PRODUCED BY THE METER FROM HIS DAILY LOGBOOK BUT WAS UNABLE TO PROVIDE EXACT TIMES FOR RESULTS: (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
151730 METRIX AIR BLOOD GLUCOSE SYSTEM NBW TRIVIDIA HEALTH, INC. METRIX AIR MT2001 00021292007447

Patients

Seq Age Sex Outcome Treatment
1 0 YR SECOND THERAPY