{
  "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": "79093",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to  PA.",
      "recall_number": "Z-0809-2018",
      "product_description": "proSA Tool Set used to adjust and verify the proSA Adjustable Shunt System    Shunt, central nervous system and components",
      "product_quantity": "2",
      "reason_for_recall": "A proSA adjusting pin used to adjust the proSA Adjustable Shunt System does not set the correct valve opening pressure.",
      "recall_initiation_date": "20170921",
      "center_classification_date": "20180301",
      "termination_date": "20180808",
      "report_date": "20180307",
      "code_info": "Batch #20034364 and #20034751"
    }
  ]
}