Facility

Savaria Lifts (UK) Ltd.

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

Key facts

1recalls · worst Class II

2inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3011268530
Establishment type	Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Location	82 First Avenue Kingswinford Dudley, GB DY6 7FJ
Registration status	Active · expires 2026
Parent company	Handicare Accessibility (owner-operator 10054974)
Brand names	2000; 1000; 950; 4000

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Powered Stairway Chair Lift
Product code PCD (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5150

Recalls & enforcement

Class IITerminated2012-11-29
Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub.

FDA inspections (2)

VAI2024-02-22
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2019-02-07
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

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.

All facilities operated by Handicare Accessibility

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 Lifts (UK) Ltd. (FEI 3011268530) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3011268530-savaria-lifts-uk-ltd/

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