Z-2060-2017Class II

Savaria SL-1000 Stairlift

Name: Z-2060-2017 Savaria SL-1000 Stairlift
Creator: Savaria Concord Lifts, Inc.
Published: 2017-04-12
License: https://open.fda.gov/license/

Savaria Concord Lifts, Inc. / initiated 2017-04-12 / Terminated / root cause: design

FDA source

Savaria Concord Lifts, Inc. began a recall of Savaria SL-1000 Stairlift on 2017-04-12. FDA classified it as Class II and gives the reason as "The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2060-2017
Classification: Class II
Status: Terminated
Initiated: 2017-04-12
Posted: 2017-05-10
Terminated: 2018-03-05
Recalling firm: Savaria Concord Lifts, Inc.
Product: Savaria SL-1000 Stairlift
Product code: PCD Powered Stairway Chair Lift
Reason for recall: The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
Root cause tag: design
FDA root cause: 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
Product codes and lots: s/n or lot number - Job Number lots 671494 - 672668

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2060-2017
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2060-2017	Class II	Terminated	Voluntary: Firm initiated	2017-05-17	2017-05-10

Product code PCD

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)