{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Algete",
      "state": "N/A",
      "country": "Spain",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81377",
      "recalling_firm": "Sedecal S.A.",
      "address_1": "Pol. Industrial Rio De Janiero",
      "address_2": "Calle Pelaya 9-13",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US and Canada",
      "recall_number": "Z-0488-2019",
      "product_description": "Sedecal NOVA FA DR System. for diagnostic radiography.",
      "product_quantity": "145 units",
      "reason_for_recall": "A safety problem with installation and maintenance could lead to the breakage of the two steel cables that support the equipment to its roof anchor.  Due to this, the equipment may fall and cause harm to the patient, user, or third parties.",
      "recall_initiation_date": "20180718",
      "center_classification_date": "20181120",
      "report_date": "20181128",
      "code_info": "Serial Numbers 07360816 through 17291024",
      "more_code_info": ""
    }
  ]
}