Facility

RECOR MEDICAL

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

Key facts

1recalls · worst Class II

1inspections · worst NAI

—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)	3010024164
Establishment type	Manufacture Medical Device
Location	1049 Elwell Ct Palo Alto, CA, US 94303
Registration status	Active · expires 2026
Parent company	Recor Medical, Inc. (owner-operator 10082465)
Brand names	Paradise Ultrasound Renal Denervation System

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Ablation Catheter, Renal Denervation
Product code QYI (opens in a new tab) · Class III · Unknown

Recalls & enforcement

Class IIOngoing2026-01-29
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.

FDA inspections (1)

NAI2023-07-11
No Action Indicated · Bioresearch Monitoring

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 Recor 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. “RECOR MEDICAL (FEI 3010024164) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3010024164-recor-medical/

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