FDA Device recall Z-0681-2022
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
- FDA Device
- Class II
- ongoing
- Published 2022-03-09
On 2022-03-09 the FDA classified a Class II recall of Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift by Acorn Stairlifts, citing the design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0681-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2016-04-20 |
| Published | 2022-03-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Acorn Stairlifts |
| Distribution | US |
Product
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Reason
The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
Identifiers
| code_info | Acorn 130/180 Seat Squab, included as part of The Acorn 130 Straight Stairlift and the Acorn 180 Curved Stairlift. Ser…Acorn 130/180 Seat Squab, included as part of The Acorn 130 Straight Stairlift and the Acorn 180 Curved Stairlift. Serial Numbers: 140110386215,140110356934,140110330295,140110410265,140110356903,140110319711,140110353380,140110358263,140110387720,140110357449,140110348263,140110380857,140110357022,140110334193,140110390695,140110348564,140110364396,140110362060,140110278902,140110360364,140110263037,140110366547,140110320108,140110372638,140110387248,140110367036,140110311884,140110405234,140110387712,140110400646,140110378178,140110393130,140110389009,140110348935,140110409990,140110413893,140110392454,140110253282,140110406587,140110367992,140110370968,140110367770,140110308838,140110387501,140110402408,140110361497,140110366632,140110365928,140110352238,140110406996,140110401030,140110382733,140110361514,140110363598,140110382800,140110387432,140110367208,140110391181,140110374800,140110370938,140110399914,140110253288,140110355287,140110405166,140110301171,140110358373,1401102867 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0681-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.