{
  "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": "98747",
      "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-1807-2026",
      "product_description": "The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.",
      "product_quantity": "480,000",
      "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": ""
    }
  ]
}