Lower riskMedical device recall · FDA · Published February 24, 2023
Tobii Dynavox TD I-110 Speech Device Recall: Battery May Come Loose
Tobii Dynavox recalls TD I-110 speech devices due to potential battery detachment. Affected units have specific serial numbers and catalog codes. Consumers should contact for remedy.
Problem maintaining the stable placement of the battery may come loose from the housing and become damaged.
Take action
Contact the company
📍Recalling firmTobii Dynavox Llc2100 Wharton St Ste Ste 400 · Pittsburgh, PA 15203-1691
✎ GovInfoNow plain-language explainer
Tobii Dynavox is recalling TD I-110 speech devices because the battery might become loose and damaged. This could pose a risk if the device falls or is mishandled. Affected users should check their serial numbers and contact the company for instructions. Read more at govinfonow.com/recall/58849-tobii-dynavox-td-i-110-speech-device-recall-battery-may.
“Tobii Dynavox TD I-110 Speech Device Recall: Battery May Come Loose.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58849-tobii-dynavox-td-i-110-speech-device-recall-battery-may. Based on FDA recall #Z-1399-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1399-2023%22&limit=1).
The FDA announced on Feb. 24, 2023, that Tobii Dynavox Llc is recalling the TD I-110 speech device due to a battery placement hazard. The agency issued recall number Z-1399-2023 for the voluntary Class II action affecting approximately 3,924 units distributed worldwide.
Serial Numbers: TD110-211005000001 through TD110-220927004400
Quantity: 3,924 units
The hazard
The device may have a problem maintaining the stable placement of the battery. The battery may come loose from the housing and become damaged.
Context
GovInfoNow's records show Tobii Dynavox Llc had one other recall on record since July 8, 2026: the TD Navio Maxi Speech Device Recall regarding battery short circuit risk. Other recent recalls of similar products include the HeartMate 11V Backup Battery Recall (May 13, 2026), the Maquet PowerLED 300 Concealed Lighting System Recall (Aug. 7, 2026), and the Fresenius Kabi Ivenix Infusion System Software Recall (May 6, 2026).
How to tell if you have this one
Check for serial numbers starting with TD110-211005000001 to TD110-220927004400. The device has catalog number 750567 and UDI 7340074601714.
Brand
Tobii Dynavox
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Serial Numbers
Look for serial numbers between TD110-211005000001 and TD110-220927004400 on the device.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1399-2023 (February 24, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1399-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.