{
  "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,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Maastricht-Airport",
      "state": "",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95188",
      "recalling_firm": "Technomed Europe",
      "address_1": "Amerikalaan 71",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US:  FL, CA, TX, IL, NY, PA, MA",
      "recall_number": "Z-3131-2024",
      "product_description": "NEUROSIGN Disposable Stimulating Dissector, REF 5888-00",
      "product_quantity": "71 units",
      "reason_for_recall": "Product has have presence of brown discoloration or substance on the hinge area of the device",
      "recall_initiation_date": "20240725",
      "center_classification_date": "20240912",
      "report_date": "20240918",
      "code_info": "UDI/DI 08718375869659, Lot Numbers:  061158, 061380",
      "more_code_info": ""
    }
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}