Facility

ERGOACTIVES, LLC

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)	3007084179
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	20725 NE 16TH AVE, STE A26 Miami, FL, US 33179
Registration status	Active · expires 2026
Parent company	Ergoactives, LLC (owner-operator 10027007)
Brand names	Tucane; Ergocane; Ergocane 2G; Ergocane 2G Black Python

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Cane, Safety Walk
Product code KHY (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3075

Recalls & enforcement

Class IITerminated2016-01-19
Products are marketed without a cleared 510k.

FDA inspections (2)

NAI2017-01-20
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2016-01-12
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 Ergoactives, LLC

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. “ERGOACTIVES, LLC (FEI 3007084179) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007084179-ergoactives-llc/

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