{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Englewood Cliffs",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81057",
      "recalling_firm": "AS Software, Inc.",
      "address_1": "560 Sylvan Ave",
      "address_2": "N/A",
      "postal_code": "07632-3119",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide.",
      "recall_number": "Z-0118-2019",
      "product_description": "AS-OBGYN Information System version 7.824.x",
      "product_quantity": "52 systems",
      "reason_for_recall": "Any change made to current ultrasound machine software or hardware upgrades, adding or modifying custom fields, or adding a new Ultrasound Machine, must be tested prior to the use in production environment to ensure that ultrasound measurements are crossing over correctly to the AS  system",
      "recall_initiation_date": "20180920",
      "center_classification_date": "20181016",
      "termination_date": "20190419",
      "report_date": "20181024",
      "code_info": "Software version 7.824.x"
    }
  ]
}