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 | Terminated |
| Reason | Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break. |
| Product | Acorn 180 Curved Stairlift |
| Quantity | 1,290 USA and 9,607 Foreign |
| Distribution | Worldwide Distribution - USA (nationwide) Distribution to the states of : AL, AZ, CA, CO, DE, FL, GA, IL, IN, KS, KY, LA, MA, ME, MD, MI, MO, NH, NJ, NY, NC, OH, PA, RI, SC, TN, TX, UT, VT, VI, WA, WV, WI, and District of Columbia and to the countries of UK and Germany. |
| Initiated | 2016-02-17 |
| Classified | 2016-04-20 |
| Terminated | 2019-01-29 |
| Recall number | Z-1530-2016 |
| 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-1530-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73509/
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