{
  "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": "West Palm Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98507",
      "recalling_firm": "Technological Medical Advancements LLC",
      "address_1": "1601 Belvedere Rd Ste E-180",
      "address_2": "",
      "postal_code": "33406-1541",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of TX, CA, MI, MD, PA, FL, MN, DC, MI.",
      "recall_number": "Z-2162-2026",
      "product_description": "Diowave Laser System, REF: Diowave 250W",
      "product_quantity": "16",
      "reason_for_recall": "Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.",
      "recall_initiation_date": "20260109",
      "center_classification_date": "20260511",
      "report_date": "20260520",
      "code_info": "UDI-DI: G180DIOWAVESTEALTHMAX0. All software versions prior to, but not including V1.81",
      "more_code_info": ""
    }
  ]
}