Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due to If the slack in the wires is not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Invacare Corporation directly.
Affected Products
FDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width configurations with power recline seating system and a conventional style back.
Quantity: 60
Why Was This Recalled?
If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight may cause the headrest knob or clamp bracket to pinch, damage or cut the wire. Smoking, sparking, burning or fire may occur if a wire is repetitively pinched at the same place.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Invacare Corporation
Invacare Corporation has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report