Permobil TiLite — Class II medical device recall Z-0264-2022
Ongoing recall by TiSport, Llc, reported 2021-11-24, distributed nationwide. Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may no
| Recall number | Z-0264-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TiSport, Llc, Pasco, WA, United States |
| Recall initiated | 2021-09-24 |
| Classified | 2021-11-18 |
| Reported by FDA | 2021-11-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, FR, GB, IE, IT, NZ, SE, UY |
| Quantity | 5,373 |
Product
Permobil TiLite, Models: Aero Z, and ZRA
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0264-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.