{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Beachwood",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65494",
      "recalling_firm": "National Biological Corp",
      "address_1": "23700 Mercantile Rd",
      "address_2": "N/A",
      "postal_code": "44122-5900",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution including the states of: AL, CA, MN, and NC.",
      "recall_number": "Z-1779-2013",
      "product_description": "Dermalight 80 Model Number UVB-083, one unit per box.    The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo.",
      "product_quantity": "6 units",
      "reason_for_recall": "The incorrect manual may have been packaged with this  product. UVB-083 devices may have included the  manual for a UVA-080 device.",
      "recall_initiation_date": "20130408",
      "center_classification_date": "20130719",
      "termination_date": "20140224",
      "report_date": "20130731",
      "code_info": "The following batch and serial numbers are affected by the recall: Batch 007778, Serial numbers D83-30016 to D83-30021.",
      "more_code_info": ""
    }
  ]
}