Medical DeviceJan 19, 2022
Ki Mobility recall — FDA Z-0467-2022
The Instructions for Use provided with the device contained information intended for use of a mechanical wheelchair, not a chair with casters.
Class IIIFDA: TerminatedKi Mobility LLC
Recall history in this database
Classification mix: Class III: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Ki Mobility LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.