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 |