{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sarasota",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80496",
      "recalling_firm": "Quasar Bio-Tech, Inc.",
      "address_1": "1465 Tallevast Rd",
      "address_2": "N/A",
      "postal_code": "34243-5036",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution to CA, FL, GA, HI, IL, LA, MD, NE, NY, OH, TX, VA, WA, WI.      Worldwide distribution to Australia, China, Netherlands, United Kingdom",
      "recall_number": "Z-2974-2018",
      "product_description": "Quasar MD Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.",
      "product_quantity": "6,783 units total",
      "reason_for_recall": "Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.",
      "recall_initiation_date": "20180629",
      "center_classification_date": "20180905",
      "termination_date": "20190827",
      "report_date": "20180912",
      "code_info": "Product Number DPA-024.  UPC Code 0 91037 46143 8"
    }
  ]
}