FDA Adverse Event Other Summary report: N

TRUE METRIX BLOOD GLUCOSE METER KIT

MDR report key: 25277847 · Received May 26, 2026

Report

Report Number
MW5188583
Event Type
Other
Date Received
May 26, 2026
Date of Event
May 8, 2026
Report Date
May 21, 2026
Manufacturer
TRIVIDIA HEALTH, INC.
Product Code
NBW
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

THE REPORTER STATED THAT THEY RECEIVED A RECALL LETTER FROM WALMART REGARDING THE TRUE METRIX BLOOD GLUCOSE METER AND IDENTIFIED THAT ONE OF THEIR SENSORS/TEST STRIP PRODUCTS WAS INCLUDED ON THE AFFECTED LIST. NO DEVICE MALFUNCTION, PATIENT INJURY, ADVERSE EVENT, OR MEDICAL INTERVENTION WAS REPORTED. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
126557 TRUE METRIX BLOOD GLUCOSE METER KIT SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER NBW TRIVIDIA HEALTH, INC.

Patients

Seq Age Sex Outcome Treatment
1 Female