{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Guilford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85178",
      "recalling_firm": "Butterfly Network, Inc.",
      "address_1": "530 Old Whitfield St",
      "address_2": "N/A",
      "postal_code": "06437-3441",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1601-2020",
      "product_description": "Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction) Tool  REF/Model: 850-20003  UDI: (01)00866646000206  Software versions 1.10.0, 1.11.0, 1.12.0, 1.13.0, 1.13.0, 1.14.0, 1.15.0    Product Usage: Intended use: Diagnostic ultrasound imaging and measurement of anatomical structures.",
      "product_quantity": "11,183",
      "reason_for_recall": "Distributed without an approved 510(k)",
      "recall_initiation_date": "20200224",
      "center_classification_date": "20200327",
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      "report_date": "20200408",
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