FDA Device recall Z-2060-2017
Savaria SL-1000 Stairlift
- FDA Device
- Class II
- terminated
- Published 2017-05-17
On 2017-05-17 the FDA classified a Class II recall of Savaria SL-1000 Stairlift by Savaria Concord Lifts, citing the electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2060-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-12 |
| Published | 2017-05-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Savaria Concord Lifts |
| Distribution | n/a |
Product
Savaria SL-1000 Stairlift
Reason
The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
Identifiers
| code_info | s/n or lot number - Job Number lots 671494 - 672668 |
|---|
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-2060-2017%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.