Acorn stairlifts recalled due to inadequate seat structural strength
Acorn Stairlifts Inc. is recalling multiple stairlift models because the seats may not have adequate strength to consistently support users during continued use, creating a fall hazard.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall involving a structural defect in a mobility device. The inadequate seat strength poses a direct risk of falls for users, matching the rubric criterion of a risk-of-harm product where injury has not yet been reported.
Plain-English summary
Acorn Stairlifts Inc. is recalling the Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift. Approximately 26,428 units are affected and were distributed nationwide.
The seats in these stairlifts do not consistently have adequate strength to support users' weight during continued use. This design defect creates a risk of seat failure and potential falls.
The affected stairlifts were distributed across all 50 states, Puerto Rico, and the Virgin Islands. Users should stop using the recalled stairlifts and contact Acorn Stairlifts Inc. for information about repair or replacement options.
The recalled product
- Product
- Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
- Manufacturer
- Acorn Stairlifts, Inc
- Category
- Medical Device — Mobility Aid
- Affected units
- 26,428
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Acorn 130/180 Seat Squab
- 140110356934
- 140110330295
- 140110410265
- 140110356903
- 140110319711
- 140110353380
- 140110358263
- 140110387720
- 140110357449
- 140110348263
- 140110380857
- 140110357022
- 140110334193
- 140110390695
- 140110348564
- 140110364396
- 140110362060
- 140110278902
- 140110360364
Distribution
Related recalls
Same manufacturer · Acorn Stairlifts, Inc
See all →- SevereAcorn 180 Curved Stairlift Recalled Due to Broken Rivets
FDA (Devices) · 2016-04-27
Same hazard · structural defect
See all →- HighCanon Medical Alphenix X-ray Systems Recalled for Loose Ceiling Screws
FDA (Devices) · 2026-09-02
- HighLight Boy Recalls GBX12SK Light Towers Due to Frame Bending Risk
NHTSA · 2026-09-01
- SevereKmaier Infant Walkers Recalled for Serious Fall Hazard
CPSC · 2026-08-27
- Highrestor3d Recalls Veritas Standard Glenoid Baseplates Due to Machining Defect
FDA (Devices) · 2026-08-26
- SevereFord Recalls 2026 Maverick, F-150, and Bronco Sport for Joint Issues
NHTSA · 2026-08-25