{
  "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": "Lancaster",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87958",
      "recalling_firm": "Exact Medical Manufacturing, Inc.",
      "address_1": "4917 William St Ste C",
      "address_2": "N/A",
      "postal_code": "14086-3200",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution to states of FL, MT, NY, OH, GA, and Puerto Rico",
      "recall_number": "Z-1918-2021",
      "product_description": "Hays Ultrasound kit\t    Item ID: H1000SE",
      "product_quantity": "10020 units",
      "reason_for_recall": "No 510k for the product to be used in a natural or surgical opening to the body",
      "recall_initiation_date": "20210429",
      "center_classification_date": "20210621",
      "termination_date": "20220526",
      "report_date": "20210630",
      "code_info": "Lot Numbers:  2005E090  2006E495"
    }
  ]
}