{
  "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": "2026-09-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "216124",
      "product_res_number": "Z-2571-2025",
      "event_date_initiated": "2025-08-29",
      "event_date_posted": "2025-09-18",
      "recall_status": "Open, Classified",
      "res_event_number": "97621",
      "product_code": "RHP",
      "product_description": "The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.",
      "code_info": "SKU BT-GERMWAND-LRG-WHT and Testing: September 8-10, 2020",
      "firm_fei_number": "3039602167",
      "recalling_firm": "BigTree Sales Inc.",
      "address_1": "11715 Clark St",
      "city": "Arcadia",
      "state": "CA",
      "postal_code": "91006-5806",
      "reason_for_recall": "The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "BigTree Sales, Inc. notified FDA and their customers as required by 21 CFR 1003.10(b), that their electronic product, Portable UV-C Light Sanitizer Wand/Travel UV Sanitizing Wand, model: HH1103/HD-UV-01PL03 (SKU BT-GERMWAND-LRG-WHT), has been discovered to contain a defect related to its safety. Their customer letter was sent with the knowledge of the U.S. Food and Drug Administration (FDA).",
      "distribution_pattern": "U.S.A",
      "openfda": {
        "device_name": "Uv Lamp, Germicidal",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}