{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hoffman Estates",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80071",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "2501 Barrington Rd",
      "address_2": "N/A",
      "postal_code": "60192-2061",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to .      International distribution to Finland, France, France, Iran, Ireland, Italy, Japan, Japan, Netherlands.",
      "recall_number": "Z-1930-2018",
      "product_description": "Biograph Horizon, PET/CT System using VJ10A, VJ10B, VJ20A scanners that provide registration and fusion of high resolution physiologic and anatomic information.",
      "product_quantity": "14 units",
      "reason_for_recall": "Possibility that the Biograph Horizon systems performing CT retrospective cardiac gating or PET cardiac gating examinations may experience a waveform sampling issue caused by a firmware change within the Universal Physiological Measurement Module.",
      "recall_initiation_date": "20180221",
      "center_classification_date": "20180524",
      "termination_date": "20181012",
      "report_date": "20180530",
      "code_info": "Code No. 10532746, 10532748"
    }
  ]
}