# FDA recall Z-2201-2020

> **Trividia Health, Inc.** · Class II · device recall initiated 2020-04-20.

## Product

TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip or forearm.

## Reason for recall

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.

## Distribution

US Nationwide distribution including in the state of Florida.

## Key facts

- **Recall number:** Z-2201-2020
- **Recalling firm:** Trividia Health, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-20
- **Report date:** 2020-06-10
- **Termination date:** 2021-06-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ft Lauderdale, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2201-2020

## Citation

> AI Analytics. FDA recall Z-2201-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2201-2020. Source: US FDA. Licensed CC0.

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