FDA Device recall Z-1530-2016
Acorn 180 Curved Stairlift
- FDA Device
- Class II
- terminated
- Published 2016-04-27
On 2016-04-27 the FDA classified a Class II recall of Acorn 180 Curved Stairlift by Acorn Stairlifts, citing aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1530-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-17 |
| Published | 2016-04-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Acorn Stairlifts |
| Distribution | US |
Product
Acorn 180 Curved Stairlift
Reason
Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
Identifiers
| code_info | Serial Numbers: 140401487591 to 140410249946. All models manufactured before April 2012 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1530-2016%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.