{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "country": "United States",
      "city": "El Segundo",
      "address_1": "2151 East Grand Avenue",
      "reason_for_recall": "Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.",
      "address_2": "",
      "product_quantity": "9432 units",
      "code_info": "Lot 36775, 36786, 36828, 36864",
      "center_classification_date": "20130511",
      "distribution_pattern": "Distributed Nationwide and in Canada.",
      "state": "CA",
      "product_description": "Electrode, cutting, 24FR (27050G/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Karl Storz Endoscopy America Inc",
      "recall_number": "Z-1305-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "55358",
      "termination_date": "20130513",
      "more_code_info": "",
      "recall_initiation_date": "20090601",
      "postal_code": "90245",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}