{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "87861",
      "product_res_number": "Z-0608-2010",
      "event_date_initiated": "2009-09-08",
      "event_date_posted": "2010-02-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-08-21",
      "res_event_number": "54226",
      "product_code": "REG",
      "product_description": "Model ST-400 Solafeet Foot portable tanners; Solafeet, Inc.\n\nUse: feet tanner.",
      "code_info": "Any codes associated with Model ST-400.",
      "firm_fei_number": "3007708365",
      "recalling_firm": "Solafeet, Inc.",
      "address_1": "W University Pkwy Unit A W University Pkwy",
      "address_2": "Unit A",
      "city": "Sarasota",
      "state": "FL",
      "postal_code": "34243-2742",
      "additional_info_contact": "941-359-2608",
      "reason_for_recall": "Product failed to have a label that contained a recommended exposure schedule; the operator's manual provided inadequate instructions for use; and label implication may result in overexposure.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "Solafeet sent letters to customers informing them that the labeling and instructions included with the product were not in accordance with the FDA requirements.  Attached with the letter was a replacement label and a replacement set of instructions.  Customers are to attach the new label on top of the old label and use the new instructions, noting the change in exposure limits.  Questions should be directed to 941-359-2608 or info@solafeet.com.",
      "product_quantity": "72 units",
      "distribution_pattern": "Nationwide Distribution",
      "openfda": {
        "device_name": "Suntan Lamp",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4635",
        "device_class": "2"
      }
    }
  ]
}