{
  "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": "Lubbock",
      "address_1": "4620 71st St",
      "reason_for_recall": "The device has the potential to be packaged in the wrong product box.",
      "address_2": "Bldg 75-77",
      "product_quantity": "32 boxes",
      "code_info": "Lot 47295",
      "center_classification_date": "20161018",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the countries of :  Colombia, Venezuela/Ecuador, Japan, India, Canada, and UK.",
      "state": "TX",
      "product_description": "Cytoplast Titanium-Reinforced Posterior Singles Membrane     A temporarily implantable material (non-resorbable) for use as a space-making barrier in the treatment of periodontal bone defects.",
      "report_date": "20161026",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Osteogenics Biomedical, Inc.",
      "recall_number": "Z-0113-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75119",
      "termination_date": "20161223",
      "recall_initiation_date": "20160907",
      "postal_code": "79424-2230",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}