{
  "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-0036-2020",
      "product_description": "TxRx Knee 15 Coil 1.5T  QED part number: Q7000056  Siemens Model # 10606828",
      "product_quantity": "36 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 #  1694  1841  1887  1933  1998  3195  3291  3292  3293  3294  3298  3299  3300  3301  3302  3303  3304  3305  3306  3307  3308  3309  3310  3311  3312  3313  3314  3315  3316  3317  3318  ¿1137  ¿1361  ¿1378  ¿1628   ¿2447"
    }
  ]
}