Use cautionMedical device recall · FDA · Published March 30, 2022
Invacare TDX SP2 Wheelchairs May Lose Power Due to Battery Wiring Issue
Invacare recalls TDX SP2 wheelchairs with specific model numbers due to risk of battery disconnection causing power loss during use or shipping. Affected units may lose power when encountering obstacles or impacts.
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.
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Contact the company
📍Recalling firmInvacare Corporation1200 Taylor St · Elyria, OH 44035-6248
✎ GovInfoNow plain-language explainer
Invacare is recalling TDX SP2 wheelchairs with model numbers TDXSP2, TDXSP2-MCG, and TDXSP2V because the battery wiring can disconnect during shipping or use, causing power loss. This could lead to the wheelchair becoming inoperable when needed. Read more at govinfonow.com/recall/60868-invacare-tdx-sp2-wheelchairs-may-lose-power-due-to-battery.
“Invacare TDX SP2 Wheelchairs May Lose Power Due to Battery Wiring Issue.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60868-invacare-tdx-sp2-wheelchairs-may-lose-power-due-to-battery. Based on FDA recall #Z-1130-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1130-2022%22&limit=1).
The FDA announced on March 30, 2022, that Invacare Corporation is recalling its TDX SP2 wheelchairs due to a battery wiring harness hazard. The agency issued the recall for devices distributed nationwide in the U.S. and in Canada.
The battery wiring harness on the recalled wheelchairs may become disconnected during shipment or use. This disconnection results in a loss of power to the wheelchair.
Context
GovInfoNow's records show Invacare Corporation has had 6 other recalls since November 16, 2018. Other recent recalls include beds with potential weld defects (January 22, 2024) and rollators with seat collapse risks (June 15, 2023). Similar product recalls involve battery issues, including Stryker's INZONE Detachment System (April 6, 2026) and Tobii Dynavox speech devices (July 8, 2026).
How to tell if you have this one
Check the model number on the wheelchair (TDXSP2, TDXSP2-MCG, or TDXSP2V) and the serial number listed in the recall notice. The affected units were sold with specific serial numbers provided in the recall details.
Brand
Invacare
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Model Number
Identify the model number on your wheelchair (TDXSP2, TDXSP2-MCG, or TDXSP2V) to determine if it is affected.
Verify Serial Number
Compare your wheelchair's serial number against the list of affected serial numbers provided in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 35 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of AK, AR, CA, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NY, OH, OR, PA, SC, TN, TX, VA, VT, WA, and WI. The country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alaska, Arkansas, California, Connecticut, Florida, Georgia, Hawaii, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, New Jersey, New York, North Carolina, North Dakota, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Vermont, Virginia, Washington, Wisconsin.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1130-2022 (March 30, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1130-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.