{
  "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": "2026-04-08",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Whitland",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79577",
      "recalling_firm": "The Magstim Company Limited",
      "address_1": "Spring Gardens",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of AR, CA, GA, KS, MA, MD, MO, NC, NJ, NW, NY, TX and Hawaii",
      "recall_number": "Z-1352-2018",
      "product_description": "Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main Filters    Product Usage For the treatment of major depressive disorders in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.",
      "product_quantity": "43",
      "reason_for_recall": "Users manuals not supplied with 4800-00T US Rapid Therapy System",
      "recall_initiation_date": "20170928",
      "center_classification_date": "20180410",
      "termination_date": "20220621",
      "report_date": "20180418",
      "code_info": "Part # 4800-00T",
      "more_code_info": ""
    }
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}