Class II — TiSport, Llc
| Recalling firm | TISPORT, LLC |
|---|---|
| Registered facility | TISPORT, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards. |
| 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. |
| Quantity | 1,452 wheelchairs |
| Distribution | Distribution was nationwide, including Puerto Rico. There was also government distribution but no military distribution. Foreign distribution was made to Canada, Australia, Brazil, China, Italy, Saudi Arabia, Switzerland, United Kingdom, and Uruguay. |
| Initiated | 2018-09-11 |
| Classified | 2019-08-20 |
| Terminated | 2022-07-29 |
| Recall number | Z-2294-2019 |
| 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-2294-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83360/
Alerts for TISPORT, LLC
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.