{
  "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": [
    {
      "country": "United States",
      "city": "Mesa",
      "address_1": "1840 S Stapley Dr Ste 200",
      "reason_for_recall": "It was discovered that a non-sterile vacuum tube is supplied within the pack, although the Instructions for Use (IFU) describe the use of a sterile vacuum tube as part of the procedure setup.",
      "address_2": "",
      "product_quantity": "6562 units",
      "code_info": "all",
      "center_classification_date": "20161213",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the countries of :Europe (Austria, France, Germany, Italy, Netherlands, Switzerland, Spain, UK)",
      "state": "AZ",
      "product_description": "Cellfina Prep Pack, Part No. CP1",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ulthera Inc",
      "recall_number": "Z-0749-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75682",
      "termination_date": "20170913",
      "more_code_info": "",
      "recall_initiation_date": "20161114",
      "postal_code": "85204-6681",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}