# FDA recall Z-2959-2026

> **Tobii Dynavox Llc** · Class II · device recall initiated 2026-07-08.

## Product

TD Navio Midi Speech Generating Device  Model/Catalog Number: 1000798

## Reason for recall

Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2959-2026
- **Recalling firm:** Tobii Dynavox Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-08
- **Report date:** 2026-08-26

- **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-2959-2026

## Citation

> MORVS. FDA recall Z-2959-2026. Retrieved 2026-10-15 from https://api.morvs.ai/recall/Z-2959-2026. Source: US FDA. Licensed CC0.

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