{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "48605",
      "product_res_number": "Z-0156-2007",
      "event_date_initiated": "2006-09-28",
      "event_date_posted": "2006-11-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-13",
      "res_event_number": "36406",
      "product_code": "MOQ",
      "product_description": "DermaStyle Chroma 2-blue and red light device indicated to be used in treating skin blemishes; portable home therapy; Lumiport LLC.",
      "code_info": "All units sold before 08/01/2006.",
      "firm_fei_number": "3005952043",
      "recalling_firm": "Lumiport, LLC",
      "address_1": "5255 North Edgewood Drive, Suite 235 5255 North Edgewood Drive",
      "address_2": "Suite 235",
      "city": "Provo",
      "state": "UT",
      "postal_code": "84604",
      "additional_info_contact": "801-804-7084",
      "reason_for_recall": "Incorrect charger; batteries may overheat , catch fire or explode while being charged with the charger enclosed with the device.",
      "root_cause_description": "Other",
      "action": "Individual customers were contacted through e-mail and/or telephone beginning 09/28/2006. They were told to stop charging and using their current DermaStyle and to destroy it to prevent accidental usage. New replacements will be mailed to all customers.",
      "product_quantity": "2480 units",
      "distribution_pattern": "World wide Distribution-sales by direct mail or internet-USA and Canada",
      "openfda": {
        "k_number": [
          "K980224",
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          "K013133"
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        "device_name": "Battery, Replacement, Rechargeable",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4820",
        "device_class": "1"
      }
    }
  ]
}