Trividia Health recalls a blood glucose meter that displays results in mmol/L instead of mg/dL, causing incorrect readings for diabetes management.
One (1) TRUE METRIX AIR blood glucose meter distributed in the United States was packaged into a TRUE METRIX blood glucose meter kit and has an incorrect factory-set unit of measure; the meter displays glucose results in mmol/L rather than mg/dL.
Trividia Health recalls a blood glucose meter that shows results in mmol/L instead of mg/dL. This error could lead to incorrect diabetes management decisions since healthcare providers typically use mg/dL for blood glucose measurements.
The meter displays glucose results in mmol/L (millimoles per liter) instead of mg/dL (milligrams per deciliter). This unit mismatch means readings are incorrect for standard diabetes care, as healthcare providers expect mg/dL measurements.
People using the TRUE METRIX blood glucose meter for diabetes monitoring. Those with diabetes who rely on accurate glucose readings are most at risk.
The recalled meter has a serial number TA1548753. It was distributed in the United States as part of a TRUE METRIX blood glucose meter kit.
Look for the serial number TA1548753 on the meter kit.
The meter displays glucose results in mmol/L instead of mg/dL, which is incorrect for diabetes management as healthcare providers use mg/dL.
The recalled meter has a serial number TA1548753 and was distributed in the United States as part of a TRUE METRIX blood glucose meter kit.
Check the serial number on the meter kit. If it matches TA1548753, contact Trividia Health for guidance.
We’ve drafted a message you can send Trividia Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2201-2020 — Trividia Health Trividia Health Hello, I own a Trividia Health that is covered by recall Z-2201-2020 from Trividia Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
