ACORN STAIRLIFTS INC
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
- Inspections (1)
Devices registered here (1)
- Powered Stairway Chair LiftProduct code PCD (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5150
Recalls & enforcement
- Class IIOngoing2016-04-20The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.
- Class IITerminated2016-02-17Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
FDA inspections (1)
- NAI2025-12-03No Action Indicated · Compliance: Devices; Postmarket Assurance: 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.
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. “ACORN STAIRLIFTS INC (FEI 3033915638) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3033915638-acorn-stairlifts-inc/
Alerts for ACORN STAIRLIFTS 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.
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.