Tobii Dynavox TD Navio Midi Speech Generating Device Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Tobii Dynavox Llc is recalling TD Navio Midi Speech Generating Devices due to potential battery mounting issues that could lead to internal short circuits.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on September 8, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
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.
Which Products Are Affected
TD Navio Midi Speech Generating Device, Model/Catalog Number: 1000798. UDI-DI 073400747602056. Serial Numbers TDNM1-240628000004 through TDNM1-260617070001. Distributed nationwide in the United States. Recall Number: Z-2959-2026. Class II recall initiated July 8, 2026.
What You Should Do
Consumers with affected devices should refer to the recalling firm for information on the issue.
Why This Matters
The potential for localized heating and gas venting poses a risk of device malfunction during use.
Source
FDA recall Z-2959-2026, Event ID 99410. Tobii Dynavox Llc, Pittsburgh, PA.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (902 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.