The Recall Desk
SevereFDA (Devices)·Z-1530-2016·Announced 2016-04-27

Acorn 180 Curved Stairlift Recalled Due to Broken Rivets

Acorn Stairlifts Inc is recalling 1,290 Acorn 180 Curved Stairlifts in the US because aluminum rivets may break under prolonged use.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall involves a structural defect (broken rivets) in a mobility device, which poses a significant risk of injury if the stairlift fails, aligning with the 'Severe' criteria for structural defects and significant injury reports.

Plain-English summary

Acorn Stairlifts Inc is recalling 1,290 units of the Acorn 180 Curved Stairlift in the United States. The recall affects all models manufactured before April 2012, with serial numbers ranging from 140401487591 to 140410249946. The product was distributed nationwide to specific states and the District of Columbia.

The recall was initiated because aluminum rivets holding the base squab to the framer were observed to elongate and subsequently break during prolonged customer use. This defect could compromise the structural integrity of the stairlift.

Consumers who own this product should stop using the stairlift and contact Acorn Stairlifts Inc for further instructions on how to resolve the issue.

The recalled product

Product
Acorn 180 Curved Stairlift
Manufacturer
Acorn Stairlifts Inc
Category
Medical Device — Mobility Aid
Hazard

Distribution

Distributed nationwide across the United States.

The notice also names 34 states specifically:

Related recalls

Same manufacturer · Acorn Stairlifts Inc

See all →

Same hazard · structural failure

See all →