{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Helsinki",
      "state": "N/A",
      "country": "Finland",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92455",
      "recalling_firm": "GE Healthcare Finland Oy",
      "address_1": "Kuortaneenkatu 2",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-2027-2023",
      "product_description": "TruSignal AllFit Sensor:    a) REF TS-AF-10, 10 pcs;   B) REF AF-25, 25 pcs; Oximeter",
      "product_quantity": "36337 devices",
      "reason_for_recall": "There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.",
      "recall_initiation_date": "20230519",
      "center_classification_date": "20230706",
      "report_date": "20230712",
      "code_info": "a) REF TS-AF-10, GTIN 0840682103176 b) REF TS-AF-25, GTIN 0840682103176"
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}