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U.S. Department of Health and Human Services

Class 2 Device Recall Savaria SL1000 Stairlift

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  Class 2 Device Recall Savaria SL1000 Stairlift see related information
Date Initiated by Firm April 12, 2017
Create Date May 10, 2017
Recall Status1 Terminated 3 on March 05, 2018
Recall Number Z-2060-2017
Recall Event ID 77050
Product Classification Powered stairway chair lift - Product Code PCD
Product Savaria SL-1000 Stairlift
Code Information s/n or lot number - Job Number lots 671494 - 672668
Recalling Firm/
Manufacturer		 Savaria Concord Lifts, Inc.
2 Walker Dr
Brampton Canada
Manufacturer Reason
for Recall		 The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
FDA Determined
Cause 2		 Component design/selection
Action The firm sent a letter to dealers dated July 26, 2016. The firm will contact consignees (distributors) via e-mail and phone.
Quantity in Commerce 1425 in the United States  734 in Canada
Distribution Distribution in the United States and Canada
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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