{
  "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": "2026-04-29",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Sunnyvale",
      "address_1": "447 Indio Way",
      "reason_for_recall": "Devices labeled for an intended use not included in the existing 510(k) or PMA, in that, the user manual contains the Indication for Use of the soma v Platinum ABUS [a 510(k) product].",
      "address_2": "",
      "product_quantity": "3 units",
      "code_info": "Serial numbers: H1280099, H1180094, B1380105",
      "center_classification_date": "20130624",
      "distribution_pattern": "Distributed in California and Illinois.",
      "state": "CA",
      "product_description": "Soma v Automated Breast Ultrasound System (ABUS), Automated Breast Ultrasound.    Indicated as an adjunct to mammography for breast cancer screening.",
      "report_date": "20130703",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "U-systems Inc",
      "recall_number": "Z-1587-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65371",
      "termination_date": "20131104",
      "more_code_info": "",
      "recall_initiation_date": "20130516",
      "postal_code": "94085-4203",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}