# FDA recall Z-1976-2019

> **Cardiocommand Inc.** · Class III · device recall initiated 2019-06-24.

## Product

TAPSYSTEM Model 2A, REF 8002A

## Reason for recall

There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly.

## Distribution

United States - AR, NM, PA, TX, and WA.

## Key facts

- **Recall number:** Z-1976-2019
- **Recalling firm:** Cardiocommand Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-24
- **Report date:** 2019-07-24
- **Termination date:** 2021-04-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1976-2019

## Citation

> AI Analytics. FDA recall Z-1976-2019. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1976-2019. Source: US FDA. Licensed CC0.

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