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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: TRIVIDIA HEALTH, INC. TRUEMETRIX; BLOOD GLUCOSE SYSTEM

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TRIVIDIA HEALTH, INC. TRUEMETRIX; BLOOD GLUCOSE SYSTEM Back to Search Results
Model Number TRUEMETRIX
Medical Device Problem Code High Test Results (2457)
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 11/18/2016
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
(b)(4).Product does not return for evaluation yet.Most likely underlying root cause of malfunction: user had an inaccurate reference.(b)(4).
 
Event or Problem Description
Costumer reported complaint for high blood glucose test results.The customer is concerned with tests results from results obtained of 237, 175 and 245 mg/dl.The customer's expected fasting blood glucose test result range is 93 - 120 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 140 mg/dl using truemetrix meter and 146 mg/dl using truemetrix meter.The product is stored according to specification in the living room.The test strip lot manufacturer's expiration date is 01/31/2018 and open vial date is (b)(6) 2016.The meter memory was reviewed for previous test result history (date / time not set correctly): (b)(6).
 
Additional Manufacturer Narrative
(b)(4).Returned meter evaluated with no defect found.Test strips not returned for evaluation.Most likely underlying root cause of malfunction: user had an inaccurate reference.(b)(4).
 
Event or Problem Description
Costumer reported complaint for high blood glucose test results.The customer is concerned with tests results from results obtained of 237, 175 and 245 mg/dl.The customer's expected fasting blood glucose test result range is 93 - 120 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 140 mg/dl using truemetrix meter and 146 mg/dl using truemetrix meter.The product is stored according to specification in the living room.The test strip lot manufacturer's expiration date is 01/31/2018 and open vial date is (b)(6) 2016.The meter memory was reviewed for previous test result history (date / time not set correctly): (b)(6).Memory concerns: all results.
 
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Brand Name
TRUEMETRIX
Common Device Name
BLOOD GLUCOSE SYSTEM
Manufacturer (Section D)
TRIVIDIA HEALTH, INC.
2400 nw 55th court
fort lauderdale FL 33309
MDR Report Key6170168
Report Number1000113657-2016-02015
Device Sequence Number730398
Product Code NBW
UDI-Device Identifier00021292007065
UDI-Public(01)00021292007065
Combination Product (Y/N)N
Initial Reporter StateNY
PMA/510(K) Number
K140100
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source consumer
Initial Reporter Occupation Other
Remedial Action Replace
Type of Report Initial,Followup
Report Date (Section B) 12/27/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Lay User/Patient
Device Expiration Date01/31/2018
Device Model NumberTRUEMETRIX
Device Catalogue NumberRE4H01-81
Device Lot NumberMT1906
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer12/19/2016
Was the Report Sent to FDA? No
Event Location Home
Type of Report(Section G)FDA Requested
Initial Date Received by Manufacturer 11/18/2016
Supplement Date Received by ManufacturerNot provided
Initial Report FDA Received Date12/13/2016
Supplement Report FDA Received Date12/27/2016
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Concomitant Medical Products
and Therapy/Usage Dates
SECOND THERAPY
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