# FDA recall Z-2479-2020

> **Preventice Services, LLC** · Class II · device recall initiated 2019-08-06.

## Product

BodyGuardian Heart Remote Monitoring Kit, consisting of two BG Heart monitors, either Models BC-1001-A or BC1001-D, and a cell phone, either Models BP1008 or BP10014, that is paired to both of the monitors.

## Reason for recall

The device data being collected and transferred to the monitoring center may not be accurate due to nonvalidated association between the phone software and the heart monitors, therefore, the patient's report should not be used to evaluate their condition.

## Distribution

US Nationwide Distribution to AK, AL, GA, NJ, OH, and TX.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-2479-2020
- **Recalling firm:** Preventice Services, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-06
- **Report date:** 2020-07-08
- **Termination date:** 2022-11-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2479-2020

## Citation

> AI Analytics. FDA recall Z-2479-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2479-2020. Source: US FDA. Licensed CC0.

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