{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Juan Capistrano",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91987",
      "recalling_firm": "DermLite LLC",
      "address_1": "31521 Rancho Viejo Rd Ste 104",
      "address_2": "",
      "postal_code": "92675-1868",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, AZ, TX, FL, NE, IA, MO, CO and the countries of Saudi Arabia, Australia, Spain.",
      "recall_number": "Z-1506-2023",
      "product_description": "DERMLITE DL4W, REF: DL4W, Rx Only MD, CE",
      "product_quantity": "32 units",
      "reason_for_recall": "Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.",
      "recall_initiation_date": "20230320",
      "center_classification_date": "20230504",
      "report_date": "20230510",
      "code_info": "Lot # 7654, serial numbers DL4WGXXXX & DL4WBXXXX (1304-1353 and 1504); UDI-DI: (01) 0 8559970",
      "more_code_info": ""
    }
  ]
}