{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lewes",
      "state": "DE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98742",
      "recalling_firm": "Uvlizer c/o RAIS INTERNATIONAL LLC",
      "address_1": "16192 Coastal Hwy",
      "address_2": "N/A",
      "postal_code": "19958-3608",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "U.S.",
      "recall_number": "Z-1808-2026",
      "product_description": "The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two peak emission wavelengths at 274 nm and 397 nm.",
      "product_quantity": "334",
      "reason_for_recall": "In some foreseeable use conditions, the products can expose nearby persons to  UVC radiation at levels significantly above limits recommended by international safety guidelines  for skin and eye exposure.",
      "recall_initiation_date": "20260306",
      "center_classification_date": "20260417",
      "report_date": "20260429",
      "code_info": "None provided.",
      "more_code_info": ""
    }
  ]
}