{
  "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": "2026-09-12",
    "results": {
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      "event_date_initiated": "2025-11-17",
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      "res_event_number": "98073",
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      "recalling_firm": "Sophysa",
      "address_1": "Rue Sophie Germain",
      "city": "Besancon",
      "country": "France",
      "reason_for_recall": "Customer complaints of Pressio monitor rebooting.",
      "root_cause_description": "Software design",
      "action": "Sophysa issued a Field Safety notice to its consignees on 11/25/2025 via email.  The notice explained the issue and requested monitoring of the patient should the unintended reboot of the monitor occur.  The consignees were directed to notify their sales representatives to schedule the monitor update.",
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}