{
  "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": "Toronto",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85216",
      "recalling_firm": "Synaptive Medical Inc",
      "address_1": "555 Richmond St West, Suite 800",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US",
      "recall_number": "Z-1759-2020",
      "product_description": "Synaptive ImageDrive Clinical",
      "product_quantity": "28 units",
      "reason_for_recall": "A software defect negatively affects the quality of images taken during diagnostic imaging (mammograms) which may result in misdiagnosis.",
      "recall_initiation_date": "20200226",
      "center_classification_date": "20200422",
      "termination_date": "20240410",
      "report_date": "20200429",
      "code_info": "ImageDrive Clinical with part number SYN-0578- all versions of the software.  With unique device identifier (UDI) #(01) 00670082000139 (10)13x1"
    }
  ]
}