{
  "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": {
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      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76210",
      "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": "USA (nationwide Distribution).",
      "recall_number": "Z-1218-2017",
      "product_description": "GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories",
      "product_quantity": "24 generators",
      "reason_for_recall": "Generators may have a faulty component which could impact the proper functioning of the device.",
      "recall_initiation_date": "20170109",
      "center_classification_date": "20170216",
      "termination_date": "20170614",
      "report_date": "20170222",
      "code_info": "Serial # 1229 1897 1898 1900  1909 1911 1929 1930  1932 1934 1938 1993  1997 1998 1999 2000  2029 2030 2031 2032  2037 2038 2039 2040  2041 2042 2045 2046  2047 2048 2049 2050  2051 2052 2168",
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