Stevens Point, WI, United States
Ki Mobility Llc recalls
1 recall recorded since 2018, most recently on 19 November 2021. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class III Medical devices
- Recall started
- 19 November 2021
- Terminated
- 31 October 2022
- Reason
- The Instructions for Use provided with the device contained information intended for use of a mechanical wheelchair, not a chair with casters.
- Distribution
- Domestic: IL, IN, KY, MI, MO, NC, SC, and TN.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0467-2022
- 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 on
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.