Class II — Acorn Stairlifts, Inc
| Recalling firm | Acorn Stairlifts Inc |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use. |
| Product | Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift |
| Quantity | 26,428 |
| 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. |
| Initiated | 2016-04-20 |
| Classified | 2022-02-28 |
| Recall number | Z-0681-2022 |
| 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 — Acorn Stairlifts, Inc (Z-0681-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88610/
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