{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "El Segundo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83419",
      "recalling_firm": "Karl Storz Endoscopy",
      "address_1": "2151 E Grand Ave",
      "address_2": "N/A",
      "postal_code": "90245-5017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: VA, MO, CA, OH, NM, NY, CO, LA, ME,  OUS: Canada",
      "recall_number": "Z-2447-2019",
      "product_description": "Flexible Intubation Fiberscope, Model # 11301AB1",
      "product_quantity": "14 scopes",
      "reason_for_recall": "The action is being initiated due to  intubation scopes improperly manufactured with a double port luer instead of a single port luer.",
      "recall_initiation_date": "20190424",
      "center_classification_date": "20190831",
      "termination_date": "20201204",
      "report_date": "20190911",
      "code_info": "Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769"
    }
  ]
}