# FDA recall Z-2294-2019

> **TiSport, Llc** · Class II · device recall initiated 2018-09-11.

## 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.

## 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.

## Key facts

- **Recall number:** Z-2294-2019
- **Recalling firm:** TiSport, Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-11
- **Report date:** 2019-08-28
- **Termination date:** 2022-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Pasco, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2294-2019

## Citation

> AI Analytics. FDA recall Z-2294-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2294-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*