{
  "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": "Orlando",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73509",
      "recalling_firm": "Acorn Stairlifts Inc",
      "address_1": "7335 Lake Ellenor Dr",
      "address_2": "N/A",
      "postal_code": "32809-6219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) Distribution to the states of :  AL, AZ, CA, CO, DE, FL, GA, IL, IN, KS, KY, LA, MA, ME, MD, MI,  MO, NH, NJ, NY, NC, OH, PA, RI, SC, TN, TX, UT, VT, VI, WA, WV, WI, and District of Columbia and to the countries of UK and Germany.",
      "recall_number": "Z-1530-2016",
      "product_description": "Acorn 180 Curved Stairlift",
      "product_quantity": "1,290 USA and 9,607 Foreign",
      "reason_for_recall": "Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.",
      "recall_initiation_date": "20160217",
      "center_classification_date": "20160420",
      "termination_date": "20190129",
      "report_date": "20160427",
      "code_info": "Serial Numbers: 140401487591 to 140410249946.  All models manufactured before April 2012"
    }
  ]
}