FDA Device recall Z-0264-2022
Permobil TiLite, Models: Aero Z, and ZRA
- FDA Device
- Class II
- ongoing
- Published 2021-11-24
On 2021-11-24 the FDA classified a Class II recall of Permobil TiLite, Models: Aero Z, and ZRA by Tisport, citing some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be configured in the right orientation to perform as intended if in….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0264-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-09-24 |
| Published | 2021-11-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Tisport |
| Distribution | US |
Product
Permobil TiLite, Models: Aero Z, and ZRA
Reason
Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be configured in the right orientation to perform as intended if involved in a motor vehicle accident. Some affected wheelchairs can no longer be used as a passenger seat until transit tie downs are replaced with redesigned transit tie downs, verified, and released to the market.
Identifiers
| code_info | Manufactured between January 19, 2017 and June 14, 2021 with the serial number range from M2005054 to 1231112011 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0264-2022%22
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