Invacare recalls TDX SP2 wheelchairs with LiNX Gyro firmware version 6.1.2 due to potential injury from aggressive deceleration. Affected models include TDXSP2, TDXSP2-CG, and others with specific UDI-DI numbers.
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
Invacare is recalling TDX SP2 power wheelchairs with LiNX Gyro Module firmware version 6.1.2 because the system may decelerate too quickly, causing injury. This affects specific models and UDI-DI numbers listed in the recall notice.
The wheelchair's LiNX Gyro system may decelerate faster than intended when running firmware version 6.1.2. This can cause the user to lose balance or fall, leading to injury.
Users of Invacare TDX SP2 power wheelchairs with LiNX Gyro Module firmware version 6.1.2 are affected. People who use these wheelchairs daily are most at risk due to potential injury from sudden deceleration.
Check if your wheelchair has model numbers like TDXSP2, TDXSP2-CG, or TDXSP2HD with UDI-DI numbers starting with 00841447100911. The firmware version should be 6.1.2.
Look for the firmware version on your wheelchair's LiNX Gyro Module. If it's 6.1.2, it's affected.
Reach out to Invacare for guidance on next steps if your wheelchair is affected.
Affected models include TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, TDXSP2X-MCG, TDXSP2V, TDXSP2V-HD, TDXSP2HD, TDXSP2HD-CG, and TDXSP2HD-MCG with specific UDI-DI numbers.
The recall notice does not specify a fix or remedy; users should contact Invacare for guidance.
Check the firmware version on your LiNX Gyro Module. If it's 6.1.2, it's affected.
We’ve drafted a message you can send Invacare to request your refund or repair — edit it as you like.
Subject: Recall Z-0445-2022 — Invacare Invacare Hello, I own a Invacare that is covered by recall Z-0445-2022 from Invacare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
