{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Guilford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85185",
      "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-1600-2020",
      "product_description": "Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentation measurement tool  REF/Model: 850-20003    Software versions 1.13.0, 1.14.0, and 1.15.0 - Product Usage: Butterfly iQ  is indicated for use by qualified and trained healthcare professionals to enable diagnostic ultrasound imaging and measurement of anatomical structures and fluids of adult and pediatric patients.",
      "product_quantity": "15,121 host devices",
      "reason_for_recall": "Distributed without an approved 510(k)",
      "recall_initiation_date": "20200224",
      "center_classification_date": "20200327",
      "termination_date": "20200612",
      "report_date": "20200408",
      "code_info": "Software versions 1.13.0, 1.14.0, and 1.15.0  UDI: (01)00866646000206"
    }
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}