TiLite X-Short anti-tip tubes — Class II medical device recall Z-2294-2019
Terminated recall by TiSport, Llc, reported 2019-08-28, distributed nationwide. The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.
| Recall number | Z-2294-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TiSport, Llc, Pasco, WA, United States |
| Recall initiated | 2018-09-11 |
| Classified | 2019-08-20 |
| Reported by FDA | 2019-08-28 |
| Terminated | 2022-07-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BR, CA, CH, CN, GB, IT, SA, UY |
| Quantity | 1,452 wheelchairs |
Product
TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs). Product Usage: The affected component is part of a manual wheelchair to provide mobility to physically impaired individuals. The affected component is used to prevent the wheelchair from tipping backwards.
Reason for recall
The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.
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-2294-2019. 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.