{
  "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": "Ongoing",
      "city": "Whitland",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81489",
      "recalling_firm": "The Magstim Company Limited",
      "address_1": "Spring Gardens",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, MA, MN, PA, TX, VA, WI, and WA",
      "recall_number": "Z-0836-2019",
      "product_description": "HORIZON Ez Arm   (Part of the HORIZON TMS Therapy System.)",
      "product_quantity": "27 (including 2 demos)",
      "reason_for_recall": "A stray strand of stainless-steel cable may  protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm.",
      "recall_initiation_date": "20181025",
      "center_classification_date": "20190214",
      "report_date": "20190220",
      "code_info": "Product #: 5162-00  Serial #'s: 55308/001, 55308/002, 55310/001, 55310/002, 55446/001, 55446/002, 55447/001, 55447-002, 55631-001, 55631-002, 55631-003, 55631-004, 55632/001, 55632/002, 55632/003, 55632/004, 55841/001, 55841-002, 55841-003, 55841-004, 55842/001, 55842/002, 55842/003, 55842/004, 55843-001, PLT00015/001 and PLT00015/002"
    }
  ]
}