{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Morton",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91335",
      "recalling_firm": "Altimate Medical, Inc.",
      "address_1": "262 W 1st St",
      "address_2": "N/A",
      "postal_code": "56270-1179",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the state of Texas.",
      "recall_number": "Z-0880-2023",
      "product_description": "ActiveAid 922, Shower/Commode Chair",
      "product_quantity": "1 unit",
      "reason_for_recall": "Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.",
      "recall_initiation_date": "20221130",
      "center_classification_date": "20230104",
      "termination_date": "20230831",
      "report_date": "20230111",
      "code_info": "Serial Number 90071504001"
    }
  ]
}