{
  "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": "Komorniki",
      "state": "",
      "country": "Poland",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89960",
      "recalling_firm": "ARJOHUNTLEIGH POLSKA Sp. z.o.o.",
      "address_1": "Ul. Ks. Piotra Wawrzyniaka 2",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and Worldwide distribution",
      "recall_number": "Z-1098-2022",
      "product_description": "Sara Plus Active Floor Lift",
      "product_quantity": "4449 devices",
      "reason_for_recall": "The device may emit smoke or ignite.",
      "recall_initiation_date": "20220405",
      "center_classification_date": "20220520",
      "termination_date": "20240905",
      "report_date": "20220601",
      "code_info": "Model Numbers:  HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001CON4869, HEP1001-US,  HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK",
      "more_code_info": ""
    }
  ]
}