TDX SP2 Base for Multiple Actuator 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
2 open recalls name at least one TDX SP2 Base for Multiple Actuator 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
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 2
We found 2 models of TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx by Invacare Corporation in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Jun 6, 2025 and Aug 7, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).
2 FDA recall records name at least one of these models by its device identifier, 2 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
Reports received per month, all models
TDX SP2 Base for Multiple Actuator 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.
- Mar 30, 2022Class IIOpen, Classified
The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The disconnection of the battery harness results in loss of power to the wheelchair.
Z-1130-2022 · Root cause: Device Design · Recall details · FDA record ↗
- 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 ↗
Most reported TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx problems
Device problems
- Improper or Incorrect Procedure or Method1
- Mechanical Problem1
- Unintended Collision1
Patient problems
- Multiple Fractures1
- No Clinical Signs, Symptoms or Conditions1
TDX SP2 Base for Multiple Actuator 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 Multiple Actuator System w/ Ultra Low Maxx TDXSP2-MCGWheelchair, powered2 recalls2 reports
- TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx TDXSP2X-MCGWheelchair, powered1 recall0 reports
Recent TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx adverse event reports
The 2 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 7, 2026Unintended Collision; Improper or Incorrect Procedure or Method
The consumer was traveling in her vehicle when she was struck by another automobile. The impact forced her secured wheelchair to break loose from its tie-downs, propelling both the consumer and the wheelchair into the front of the vehicle. This incident resulted in bodily injury to the consumer which included rib fractures, a right femur fracture, a right ankle fracture, and bilateral tibia/fibula fractures. The consumer was admitted to the hospital for 3 months.
Patient problems: Multiple Fractures
MAUDE report 50178342 ↗MalfunctionJun 6, 2025Mechanical Problem; Mechanical Problem
ON A TDXSP2-MCG POWER WHEELCHAIR, THE BRAKE LEVERS ARE SPINNING IN CIRCLES AND NOT CATCHING/ENGAGING FROM DRIVE TO FREE WHEEL MODE. THE USER WENT OVER A BUMP AND SOMEHOW THE COUPLING SWITCHED TO FREE WHEEL WHILE IN THE MIDDLE OF THE STREET. A PERSON GOT OUT OF THEIR CAR AND HELPED PUSH THE USER IN THE WHEELCHAIR ONTO THE SIDEWALK. THERE WAS NO INJURY TO THE USER, HOWEVER, THEY EXPRESSED THEY WERE SLIGHTLY SCARED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22160032 ↗
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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