Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Ki Mobility Recalled by Ki Mobility Llc Due to The Instructions for Use provided with the device...
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 Ki Mobility Llc directly.
Affected Products
Ki Mobility, Little Wave Tyke (Weight Limit: 95 lbs), Specifically the IFU The Little Wave Tyke is a manually operated device that can be used for medical purposes and is used to assist a disabled person to move from one place to another while sitting. Intended to be used by persons up to 95 pounds for transport.
Quantity: 33 units shipped with affected manuals
Why Was This Recalled?
The Instructions for Use provided with the device contained information intended for use of a mechanical wheelchair, not a chair with casters.
Where Was This Sold?
This product was distributed to 8 states: IL, IN, KY, MI, MO, NC, SC, TN
About Ki Mobility Llc
Ki Mobility Llc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report