TRIVIDIA HEALTH, INC.
4 recall(s) on record — most severe on record: Class I.
Recalls by year
- Recalls (4)
Registered facilities (2)
- Trividia Health, Inc. FEI 1000113657 · FL
- Trividia Health Taiwan, INC. FEI 3002806387 · TW
Recalls & enforcement
- Class IOngoing2026-02-06The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code cou…
- Class IIOngoing2025-10-07Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to inappropriate treatment decisions for diabetes management.
- Class IITerminated2020-04-20One (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.
- Class IIOngoing2016-06-28Product gives incorrect low blood glucose levels.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “TRIVIDIA HEALTH, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9000560-trividia-health-inc/
Alerts for TRIVIDIA HEALTH, INC.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.