Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Savaria SL-1000 Stairlift Recalled by Savaria Concord Lifts, Inc. Due to The electrical controller, combined with motor, causes feedback,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Savaria Concord Lifts, Inc. directly.
Affected Products
Savaria SL-1000 Stairlift
Quantity: 1425 in the United States 734 in Canada
Why Was This Recalled?
The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
Where Was This Sold?
Distribution in the United States and Canada
About Savaria Concord Lifts, Inc.
Savaria Concord Lifts, Inc. has 3 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report