{
  "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": "Yorba Linda",
      "address_1": "22715/22725 Savi Ranch Pkwy",
      "reason_for_recall": "The recall was initiated because there is a potential for malfunction of the OsseoCare Pro when used with the OseeoCare Pro iPad application software release 1.2.0.7.",
      "address_2": "",
      "product_quantity": "1082 (391 US)",
      "code_info": "Model Numbers: 1600870-001, 1700470-001, 1700471-001.",
      "center_classification_date": "20131113",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) United States and Internationally to Austria, Belgium, Brazil, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Hong Kong, Hungary, India, Ireland, Italy, Japan, Latvia, Lithuania, Luxembourg, Mexico, Netherlands, Norway, Philippines, Poland, Portugal, Romania, Russia, South Africa, Spain, Sweden, Switzerland, Turkey, and the United Kingdom.",
      "state": "CA",
      "product_description": "Osseocare Pro Console & Set Osseocare Pro, Model 1600870-001, 1700470-001, and 1700471-001.    Device Name: Osseocare Pro console & Set Osseocare Pro.  Model: 1600870-001, 1700470-001, 1700471-001.  Marketing status: Class I, under K092214.  Device description: Software-based, electronically controlled tabletop device.    In dentistry for dental surgery, endodontics and implantology.",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Nobel Biocare Usa Llc",
      "recall_number": "Z-0273-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66664",
      "termination_date": "20140410",
      "more_code_info": "",
      "recall_initiation_date": "20131024",
      "postal_code": "92887",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}