FDA Device recall Z-1399-2023
Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities
- FDA Device
- Class II
- ongoing
- Published 2023-04-26
On 2023-04-26 the FDA classified a Class II recall of Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities by Tobii Dynavox, citing problem maintaining the stable placement of the battery may come loose from the housing and become damaged.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1399-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-24 |
| Published | 2023-04-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Tobii Dynavox |
| Distribution | US |
Product
Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 750567
Reason
Problem maintaining the stable placement of the battery may come loose from the housing and become damaged.
Identifiers
| code_info | UDI: 7340074601714 Serial Numbers: TD110-211005000001 through TD110-220927004400 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1399-2023%22
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