{
  "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": "El Segundo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95975",
      "recalling_firm": "Karl Storz Endoscopy",
      "address_1": "2151 E Grand Ave",
      "address_2": "",
      "postal_code": "90245-5017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1061-2025",
      "product_description": "KARL STORZ - ENDOSKOPE, REF: 27000K, Ureteroscope, 7 Fr., 6¿, 34 cm, NON STERILE, RxONLY,  CE 0123",
      "product_quantity": "82 units",
      "reason_for_recall": "Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.",
      "recall_initiation_date": "20241219",
      "center_classification_date": "20250130",
      "report_date": "20250205",
      "code_info": "All Lots/UDI:04048551310816",
      "more_code_info": ""
    }
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}