{
  "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": "2026-03-18",
    "results": {
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      "city": "Provo",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91221",
      "recalling_firm": "PHONESOAP",
      "address_1": "1837 S East Bay Blvd Ste 201",
      "address_2": "",
      "postal_code": "84606-5530",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0457-2023",
      "product_description": "The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.",
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      "reason_for_recall": "Excessive ultraviolet-C radiation",
      "recall_initiation_date": "20220830",
      "center_classification_date": "20221216",
      "report_date": "20221228",
      "code_info": "SurfaceSoap UV Disinfecting Wand",
      "more_code_info": ""
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}