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 | 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. |
| Product | TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799 |
| Distribution | US Nationwide distribution. |
| Initiated | 2026-07-08 |
| Classified | 2026-08-14 |
| Recall number | Z-2960-2026 |
| 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-2960-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99410/
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