Class II — Tobii Dynavox Llc
| Recalling firm | Tobii Dynavox LLC |
|---|---|
| Registered facility | DYNAVOX Group AB (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Problem maintaining the stable placement of the battery may come loose from the housing and become damaged. |
| Product | Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 750567 |
| Quantity | 3924 units |
| 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. |
| Initiated | 2023-02-24 |
| Classified | 2023-04-18 |
| Recall number | Z-1399-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Tobii Dynavox Llc (Z-1399-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91884/
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