# FDA recall Z-0681-2022

> **Acorn Stairlifts, Inc** · Class II · device recall initiated 2016-04-20.

## Product

Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift

## Reason for recall

The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.

## Distribution

Distributed nationwide to AL, AK, AZ, AR, CA, CO, CT, DE, DC, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, VI, WA, WV, WI, and WY, as well as Puerto Rico and the Virgin Islands.    There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-0681-2022
- **Recalling firm:** Acorn Stairlifts, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2016-04-20
- **Report date:** 2022-03-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Belle Isle, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0681-2022

## Citation

> AI Analytics. FDA recall Z-0681-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0681-2022. Source: US FDA. Licensed CC0.

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