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.
“Trivid: TRUE METRIX Blood Glucose Meter Shows Results in mmol/L Instead of mg/dL.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65349-trivid-true-metrix-blood-glucose-meter-shows-results-in-mmol. Based on FDA recall #Z-2201-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2201-2020%22&limit=1).
The FDA announced on April 20, 2020, that Trividia Health, Inc. recalled one TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM because the meter displays glucose results in mmol/L instead of mg/dL. The agency stated the unit was distributed nationwide.
How to tell if you have it
Brand: Trividia Health
Product: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM
Serial Number: TA1548753
The hazard
One TRUE METRIX AIR blood glucose meter was packaged into a TRUE METRIX blood glucose meter kit with an incorrect factory-set unit of measure. The meter displays glucose results in mmol/L rather than mg/dL.
Context
GovInfoNow's records show Trividia Health, Inc. has two other recalls on record since October 7, 2025. On February 6, 2026, the company recalled blood glucose device owner booklets that may not guide users on responding to an E-5 error code. On October 7, 2025, Trividia Health recalled a blood glucose meter with display issues causing potential misreading of glucose values. Other recent recalls of similar products include Abbott Diabetes Care FreeStyle Libre 3 Plus Sensor Recall (November 24, 2025).
How to tell if you have this one
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.
Brand
Trividia Health
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Meter Serial Number
Look for the serial number TA1548753 on the meter kit.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution including in the state of Florida.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2201-2020 (April 20, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2201-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.