Acorn 180 Curved Stairlift — Class II medical device recall Z-1530-2016
Terminated recall by Acorn Stairlifts Inc, reported 2016-04-27, distributed nationwide. Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and su
| Recall number | Z-1530-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Acorn Stairlifts Inc, Orlando, FL, United States |
| Recall initiated | 2016-02-17 |
| Classified | 2016-04-20 |
| Reported by FDA | 2016-04-27 |
| Terminated | 2019-01-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, GB |
| Reason classes | device malfunction |
| Serial numbers | 140401487591, 140410249946 |
Product
Acorn 180 Curved Stairlift
Reason for recall
Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
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-1530-2016. 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.