{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Yangjiangyangjiang",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89050",
      "recalling_firm": "MAX LUX CORP",
      "address_1": "03e 01 01 Yangxi Indust",
      "address_2": "Ry Zone",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0246-2022",
      "product_description": "The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.",
      "product_quantity": "9900 units",
      "reason_for_recall": "Excessive ultraviolet-C radiation",
      "recall_initiation_date": "20211026",
      "center_classification_date": "20211129",
      "report_date": "20211208",
      "code_info": "Safe-T Lite",
      "more_code_info": ""
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}