{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Algete",
      "state": "",
      "country": "Spain",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97075",
      "recalling_firm": "SEDECAL SA",
      "address_1": "Pelaya, 9 Pol.",
      "address_2": "Pol. Ind. Rio De Janeiro",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US:  CA, IL, and NJ",
      "recall_number": "Z-0275-2026",
      "product_description": "Model Number SM-40HF-B-D-C; 40KW CANON READY, Mobile X-ray system",
      "product_quantity": "1 unit",
      "reason_for_recall": "Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.",
      "recall_initiation_date": "20250610",
      "center_classification_date": "20251023",
      "report_date": "20251029",
      "code_info": "UDI/DI 08436046001510, Serial Numbers: G41234",
      "more_code_info": ""
    }
  ]
}