# FDA recall Z-2736-2018

> **Hudson Scientific LLC** · Class II · device recall initiated 2018-07-02.

## Product

iTOVi Tracker/Scanner, Model Nos. ITS10 and ITS15  Intended to rank galvanic skin response measurements. The results are used by the software to generate a report that then makes a recommendation on nutritional supplements.

## Reason for recall

The device and its accessories may not have been manufactured according to current Good Manufacturing Practices. In addition, the firm has received three complaints regarding electric shocks received when using the device.

## Distribution

Nationwide distribution. Worldwide distribution.

## Key facts

- **Recall number:** Z-2736-2018
- **Recalling firm:** Hudson Scientific LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-02
- **Report date:** 2018-08-15
- **Termination date:** 2020-01-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hudson, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2736-2018

## Citation

> AI Analytics. FDA recall Z-2736-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2736-2018. Source: US FDA. Licensed CC0.

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