{
  "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": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75558",
      "recalling_firm": "Hologic, Inc",
      "address_1": "250 Campus Dr",
      "address_2": "N/A",
      "postal_code": "01752-3020",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide) and Internationally to Finland and Austria.",
      "recall_number": "Z-0655-2017",
      "product_description": "SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices.  SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices.    For uterine sound",
      "product_quantity": "600  units (US) ; 24 units (OUS)",
      "reason_for_recall": "Breach in sterile barrier compromising product sterility",
      "recall_initiation_date": "20161028",
      "center_classification_date": "20161122",
      "termination_date": "20170818",
      "report_date": "20161130",
      "code_info": "Lot Code US:  16E25RC  16E25RD  16F16R    Lot Code OUS:  16E25RB"
    }
  ]
}