Facility

CANARY MEDICAL USA LLC

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

Key facts

1recalls · worst Class II

—inspections in our data

—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)	3015802419
Establishment type	Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198
Location	2710 Loker Ave. West, Suite 350 Carlsbad, CA, US 92010
Registration status	Active · expires 2026
Parent company	Canary Medical, Inc. (owner-operator 10082445)
Brand names	Canturio® Smart Extension 14mm (D) x 30mm (H)

Activity by year

Recalls (1)

Devices registered here (1)

Implantable Post-Surgical Kinematic Measurement Knee Device
Product code QPP (opens in a new tab) · Class II · Orthopedic · 21 CFR 888.3600

Recalls & enforcement

Class IIOngoing2025-05-02
Due to labeling error. Product incorrectly labeled.

All facilities operated by Canary Medical, Inc.

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. “CANARY MEDICAL USA LLC (FEI 3015802419) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3015802419-canary-medical-usa-llc/

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