{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Marlborough",
      "address_1": "250 Campus Dr",
      "reason_for_recall": "Incorrect label on the Sertera Biopsy Kit",
      "address_2": "",
      "product_quantity": "570 units",
      "code_info": "Lot number: 15C10RA.",
      "center_classification_date": "20160921",
      "distribution_pattern": "Nationwide.",
      "state": "MA",
      "product_description": "Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hologic, Inc",
      "recall_number": "Z-2869-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74989",
      "termination_date": "20170203",
      "more_code_info": "",
      "recall_initiation_date": "20160822",
      "postal_code": "01752-3020",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}