{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "El Segundo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84896",
      "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: AL, AZ, CA, CO, CT, DE, FL, GA, IL, IN, MA, MD, MI, MN,  MO, NC, NH, NJ, OH, OR, PA, SC, TN, TX,  VA, WA, WI, WV,  OUS: Canda",
      "recall_number": "Z-1531-2020",
      "product_description": "Karl Storz,  Model # 11161C2, Flexible Neuroscope",
      "product_quantity": "42 scopes",
      "reason_for_recall": "During a complaint investigation it was determined that an error was  observed within the instruction manual included with some scopes. Specifically, The Quick Connector Kits (QCK) and tray information, specified for the STERIS System 1E (SS1E) sterilization method within the instruction manual is incorrect.  If the user uses SS1E to sterilize the impacted scopes and referred to the manual concerning the QCK information, the sterility of reprocessed scope cannot be guaranteed.",
      "recall_initiation_date": "20190827",
      "center_classification_date": "20200320",
      "report_date": "20200401",
      "code_info": "All Lots",
      "more_code_info": ""
    }
  ]
}