{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70086",
      "recalling_firm": "Aesculap, Inc.",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "recall_number": "Z-1012-2015",
      "product_description": "Miethke Shunt System accessories      Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.",
      "product_quantity": "772",
      "reason_for_recall": "Some Miethke Shunt System accessories may have an incorrect MR safety symbol on the shelf box label. The label should have NO symbol but instead is marked with the MR conditional symbol. The product is MR unsafe. This information is only required to be in the Instructions for Use (IFU).",
      "recall_initiation_date": "20141217",
      "center_classification_date": "20150126",
      "termination_date": "20161213",
      "report_date": "20150204",
      "code_info": "material numbers: FV400T  FV401T  FV402T  FV403T  FV404T  FV405T  FV406T  FV407T  FV408T  FV409T  FV499T  FV790T  FV791T  FV792T  FV793T  FV794T  FV795T  FV796T"
    }
  ]
}