RegWardenFDA facility compliance records
Facility

SAVARIA CONCORD LIFTS INC.

3 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2016: 1 warning letters; 2017: 3 recalls; 2023: 1 inspections12016320172018201920202021202212023202420252026
  • Recalls (3)
  • Inspections (1)
  • Warning letters (1)

Devices registered here (1)

Recalls & enforcement

  • Class IITerminated2017-04-12
    Savaria 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 .
  • Class IITerminated2017-04-12
    The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
  • Class IITerminated2017-04-12
    Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts can come loose causing the carriage to separate from the trolley and the unit to fail

FDA inspections (1)

  • NAI2023-11-02
    No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

FDA warning letters (1)

Source: U.S. FDA Compliance Actions Dashboard (opens in a new tab) (device warning letters, 2016–present). Data as of 2026-10-06. Each link opens an FDA search for the letter; FDA can take several weeks to post a letter, so a very recent one may not appear yet.

Related

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

Cite this record

RegWarden. “SAVARIA CONCORD LIFTS INC. (FEI 3005753836) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005753836-savaria-concord-lifts-inc/

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