{
  "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
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67174",
      "recalling_firm": "Aesculap, Inc.",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of  AZ, MD, MA, WI, MI, MN, DE, KS, and FL., and the countries of Australia, Germany, Great Britain, Norway and Japan.",
      "recall_number": "Z-0989-2014",
      "product_description": "Aesculap proSA Adjustment Disc Size Large (L)    The Miethke proSA Adjustment shunt system is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.",
      "product_quantity": "79",
      "reason_for_recall": "The accuracy is out of specification for the Aesculap proSA Adjustment Disc Size L.",
      "recall_initiation_date": "20131223",
      "center_classification_date": "20140219",
      "termination_date": "20141001",
      "report_date": "20140226",
      "code_info": "4 lots: 4505268906, 4505336973, 4505408485, 4505238953",
      "more_code_info": ""
    }
  ]
}