TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx TDXSP2-MCGRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841447100966), 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 this device's 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. 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 ↗

2. 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 · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, 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 ↗