{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Palo Alto",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98365",
      "recalling_firm": "ReCor Medical Inc.",
      "address_1": "1049 Elwell Ct",
      "address_2": "",
      "postal_code": "94303-4308",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA, CO, FL, KS, MO, NC, OH, TX, and VA.",
      "recall_number": "Z-1655-2026",
      "product_description": "Brand Name: Paradise¿ Ultrasound Renal Denervation System  Product Name: Paradise ¿ Catheter  Model/Catalog Number: PRDS-068-02  Product Description: Common name: Ablation catheter renal denervation",
      "product_quantity": "24",
      "reason_for_recall": "Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.",
      "recall_initiation_date": "20260129",
      "center_classification_date": "20260327",
      "report_date": "20260408",
      "code_info": "Lot Code: Model No PRDS-068-02; UDI-DI 00810008950043; Lot Number: M4862",
      "more_code_info": ""
    }
  ]
}