TDX SP2 Base for Single Act. System w/ Ultra Low MaxxRecalls & reported problems across all models
Invacare Corporation · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one TDX SP2 Base for Single Act. System w/ Ultra Low Maxx model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of TDX SP2 Base for Single Act. System w/ Ultra Low Maxx by Invacare Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
TDX SP2 Base for Single Act. System w/ Ultra Low Maxx recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 12, 2021Class IIOpen, Classified
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury
Z-0445-2022 · Root cause: Software design · names 2 of these models · Recall details · FDA record ↗
TDX SP2 Base for Single Act. System w/ Ultra Low Maxx models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- TDX SP2 Base for Single Act. System w/Ultra Low Maxx TDXSP2-CGWheelchair, powered1 recall0 reports
- TDX SP2 Base for Single Act. System w/ Ultra Low Maxx TDXSP2X-CGWheelchair, powered1 recall0 reports
Other Invacare Corporation products
All Invacare Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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