Class II — TiSport, Llc
| Recalling firm | TISPORT, LLC |
|---|---|
| Registered facility | TISPORT, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | Permobil TiLite, Models: Aero Z, and ZRA |
| Quantity | 5373 |
| Distribution | US Nationwide Distribution: MD, PA, VA, IN, NY, MO, AR, NE, NJ, WA, NM, IL, CA, OH, KY, LA, OK, WI, TX, NC, SD, MN, MA, OR; OUS (Foreign): AUSTRALIA, CANADA, FRANCE, GERMANY, IRELAND, ITALY, UNITED KINGDOM, URUGUAY, NEW ZEALAND, IRELAND, SWEDEN |
| Initiated | 2021-09-24 |
| Classified | 2021-11-18 |
| Recall number | Z-0264-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — TiSport, Llc (Z-0264-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88718/
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