{
  "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": "Mayfield Village",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83775",
      "recalling_firm": "Quality Electrodynamics LLC",
      "address_1": "6655 Beta Dr Ste 100",
      "address_2": "N/A",
      "postal_code": "44143-2380",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US in the states: NC  OUS: Germany",
      "recall_number": "Z-0033-2020",
      "product_description": "TxRx CP Extremity Coil 3T  QED part number: Q7000019  Siemens Model # 10185464",
      "product_quantity": "5 units",
      "reason_for_recall": "Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.",
      "recall_initiation_date": "20190820",
      "center_classification_date": "20191003",
      "termination_date": "20200526",
      "report_date": "20191009",
      "code_info": "Serial #  1308  1309  1310  1311  1313"
    }
  ]
}