Facility

Acorn Stairlifts, Inc

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

Key facts

2recalls · worst Class II

5inspections · 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)	3003124453
Establishment type	Manufacture Medical Device
Location	7001 Lake Ellenor Dr Belle Isle, FL, US 32809
Registration status	Active · expires 2026
Parent company	Acorn Stairlifts Inc (owner-operator 10046507)
Brand names	Brooks 120 Slimline Stairlift; Acorn 120 Outdoor Stairlift; Acorn Outdoor Stairlift; Brooks 120 Superglide Stairlift; Acorn 120 Stairlift; Brooks Outdoor Stairlift; Acorn 120 Superglide Stairlift; Acorn 120 Slimline Stairlift; Brooks 120 Stairlift; Acorn 80 Stairlift; Brooks 130 Stairlift; Acorn 180 Stairlift

Activity by year

Recalls (2)
Inspections (5)

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 IIOngoing2016-04-20
The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
Class IITerminated2016-02-17
Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.

FDA inspections (5)

NAI2025-06-05
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2023-05-12
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2021-07-16
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2018-09-04
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2016-12-09
No 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.

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. “Acorn Stairlifts, Inc (FEI 3003124453) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003124453-acorn-stairlifts-inc/

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