SAVARIA CONCORD LIFTS INC.
3 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (3)
- Inspections (1)
- Warning letters (1)
Devices registered here (1)
- Transport, Patient, PoweredProduct code ILK (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5150
Recalls & enforcement
- Class IITerminated2017-04-12Savaria 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 IITerminated2017-04-12The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire.
- Class IITerminated2017-04-12Savaria 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)
- NAI2023-11-02No 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)
- Warning Letter2016-08-03Warning Letter (opens in a new tab) · Brampton
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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