Acorn 130 Stairlift — Class II medical device recall Z-0681-2022
Ongoing recall by Acorn Stairlifts, Inc, reported 2022-03-09, distributed nationwide. The design of the seats did not consistently have the adequate strength required to support the customers weig
| Recall number | Z-0681-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Acorn Stairlifts, Inc, Belle Isle, FL, United States |
| Recall initiated | 2016-04-20 |
| Classified | 2022-02-28 |
| Reported by FDA | 2022-03-09 |
| Distributed | Nationwide (US) |
| Quantity | 26,428 |
| Reason classes | potency |
| UPC / GTIN / UDI-DI | 00140110248999, 00140110249002, 00140110249118, 00140110249125, 00140110249989, 00140110249996, 00140110250022, 00140110250107, 00140110250121, 00140110250138, 00140110250145, 00140110252552, 00140110252569, 00140110252613, 00140110252620, 00140110252637, 00140110252644, 00140110252651, 00140110252712, 00140110252750, 00140110252880, 00140110252897, 00140110252903, 00140110253146, 00140110253160 and 475 more |
| Serial numbers | 0110366042, 0319840, 10396136, 1401, 14011, 140110, 140110248994, 140110248995, 140110248997, 140110248999, 140110249000, 140110249001, 140110249002, 140110249003, 140110249004, 140110249007, 140110249008, 140110249010, 140110249011, 140110249012, 140110249015, 140110249021, 140110249023, 140110249024, 140110249025 and 475 more |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0681-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.