RegWardenFDA facility compliance records
Recall

Class II — Savaria Concord Lifts, Inc.

Recalling firmSAVARIA CONCORD LIFTS INC.
Registered facilitySAVARIA CONCORD LIFTS INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonSavaria Concord Lifts has decided to initiate a recall of the Stairfriend, because of product defect. The product defect relates to poor quality of welding holding the seat post .
ProductThe Savaria Stairfriend is a Residential, commercial, indoor, stair lift for curved stairs.
Quantity226
DistributionNorth America / South America, please see attached list.
Initiated2017-04-12
Classified2017-04-26
Terminated2017-10-16
Recall numberZ-1882-2017
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Savaria Concord Lifts, Inc. (Z-1882-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77042/

Not open yet

Alerts for SAVARIA CONCORD LIFTS INC.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.