# FDA recall Z-1399-2023

> **Tobii Dynavox Llc** · Class II · device recall initiated 2023-02-24.

## Product

Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for  ambulatory people with disabilities.  Catalog #:  750567

## Reason for recall

Problem maintaining the stable placement of the battery  may come loose from the housing and become damaged.

## Distribution

Worldwide distribution - US Nationwide and the countries of Argentina, Australia,  Belgium, Brazil, Canada, Croatia, Denmark, Estonia, Finland, France, Germany, Iceland Ireland, Italy, Latvia, Netherlands, Norway, Saudi Arabia, Slovakia, Slovenia, Sweden,  United Arab Emirates, United Kingdom.

## Key facts

- **Recall number:** Z-1399-2023
- **Recalling firm:** Tobii Dynavox Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-24
- **Report date:** 2023-04-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Pittsburgh, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1399-2023

## Citation

> AI Analytics. FDA recall Z-1399-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1399-2023. Source: US FDA. Licensed CC0.

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