{
  "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": "75937",
      "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": "Nationwide Distribution",
      "recall_number": "Z-0947-2017",
      "product_description": "Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life  The Gomco clamp is intended to be used for circumcision surgeries",
      "product_quantity": "437 units",
      "reason_for_recall": "Aesculap has received complaints of excessive bleeding after use of Gomco Circumcision Clamps.",
      "recall_initiation_date": "20161028",
      "center_classification_date": "20170105",
      "termination_date": "20180130",
      "report_date": "20170111",
      "code_info": "Material Code MG096R \u0013 (1.1 CM)  MG097R \u0013 (1.3 CM)  MG227 (1.45CM)  MG228 \u0013 (1.6CM)  MG229 \u0013 (2.1 CM)  MG230 \u0013 (2.6CM)"
    }
  ]
}