Recall Z-2060-2017— Savaria Concord Lifts, Inc.
Class II · Terminated
Class II FDA medical device recall by Savaria Concord Lifts, Inc., initiated 2017-04-12, terminated 2018-03-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Savaria SL-1000 Stairlift. Reason: The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire..
- Recalling firm
- Savaria Concord Lifts, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-04-12
- Terminated
- 2018-03-05
- Firm location
- Brampton, N/A, Canada
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.