{
  "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": "76769",
      "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": "Letter",
      "distribution_pattern": "Product was distributed throughout the United States and Canada.",
      "recall_number": "Z-1814-2017",
      "product_description": "AESCULAP MINOP InVent 30 Trocar System, non-sterile      Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.",
      "product_quantity": "21 units distributed in U.S.",
      "reason_for_recall": "Aesculap Implant Systems LLC is recalling the Minop Trocar due to the  possibility it may have sharp edges on the distal end which may lead to the abrasion of the insulation when removing the electrode.",
      "recall_initiation_date": "20170307",
      "center_classification_date": "20170412",
      "termination_date": "20180216",
      "report_date": "20170419",
      "code_info": "Item # FH620R",
      "more_code_info": ""
    }
  ]
}