{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Besancon",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98073",
      "recalling_firm": "Sophysa",
      "address_1": "Rue Sophie Germain",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide distribution in the states of  AZ, WI, TX, OR, CA, OK, ID, FL, NJ.",
      "recall_number": "Z-1029-2026",
      "product_description": "The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor",
      "product_quantity": "105 units",
      "reason_for_recall": "Customer complaints of Pressio monitor rebooting.",
      "recall_initiation_date": "20251117",
      "center_classification_date": "20260108",
      "report_date": "20260114",
      "code_info": "UDI/DI 03760124132076, All monitors",
      "more_code_info": ""
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}