Savaria SL-1000 Stairlift — Class II medical device recall Z-2060-2017
Terminated recall by Savaria Concord Lifts, Inc., reported 2017-05-17. The electrical controller, combined with motor, causes feedback, damaging a component on the control board, st
| Recall number | Z-2060-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Savaria Concord Lifts, Inc., Brampton, N/A, Canada |
| Recall initiated | 2017-04-12 |
| Classified | 2017-05-10 |
| Reported by FDA | 2017-05-17 |
| Terminated | 2018-03-05 |
| Countries outside the US | CA |
| Quantity | 1,425 in |
| Lot numbers | 671494, 672668 |
Product
Savaria SL-1000 Stairlift
Reason for recall
The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
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-2060-2017. 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.