# FDA recall Z-0264-2022

> **TiSport, Llc** · Class II · device recall initiated 2021-09-24.

## 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.

## 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

## Key facts

- **Recall number:** Z-0264-2022
- **Recalling firm:** TiSport, Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-09-24
- **Report date:** 2021-11-24

- **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-0264-2022

## Citation

> AI Analytics. FDA recall Z-0264-2022. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-0264-2022. Source: US FDA. Licensed CC0.

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