{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Saint Petersburg",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92217",
      "recalling_firm": "J&T Health and Wellness LLC",
      "address_1": "2442 23rd St N",
      "address_2": "N/A",
      "postal_code": "33713-4018",
      "voluntary_mandated": "N/A",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US",
      "recall_number": "Z-2636-2023",
      "product_description": "ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device",
      "product_quantity": "12 units",
      "reason_for_recall": "In some cases the communication isolator installed in the Model 52X can cause a disturbance in the glass-filter safety circuit.",
      "recall_initiation_date": "20230331",
      "center_classification_date": "20230928",
      "report_date": "20231004",
      "code_info": "52X0012, 52X0013, 52X0014, 52X0024, 52X0029, 52X0030, 52X0031, 52X0032, 52X0033, 52X0034, 52X0036,  52X0037"
    }
  ]
}