{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lasnitzhohe",
      "state": "",
      "country": "Austria",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82796",
      "recalling_firm": "I.T.S. GmbH",
      "address_1": "Autal 28",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US nationwide distribution in the states of Florida and Puerto Rico, and countries of Austria, Netherlands, Slovenia, South Africa, Switzerland.",
      "recall_number": "Z-1718-2019",
      "product_description": "Rim Plate, 10-Hole, Left, PRS RX System.  Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolidation has taken place. After this, the implant has no more use and can be removed.",
      "product_quantity": "65 devices",
      "reason_for_recall": "The titanium implant has the wrong article number laser marked on it.",
      "recall_initiation_date": "20190509",
      "center_classification_date": "20190604",
      "report_date": "20190612",
      "code_info": "Model Number: 21206-10;  Lot Code: 26/F42778",
      "more_code_info": ""
    }
  ]
}