{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Jena",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70365",
      "recalling_firm": "Carl Zeiss Meditec AG",
      "address_1": "Carl Zeiss Promenade 10",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1049-2015",
      "product_description": "FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and  v 3.2,  v 3.2.1.(DVD and USB Flash Drive Format).  Catalog numbers:  000000-20107-750 (DVD with either FORUM v 3.1 or v 3.1.1)  000000-2058-601 (DVD with either FORUM v 3.2 or 3.2.1);  000000-2084-928 (USB drive with FORUM 3.2.1)    Ophthalmic image management system.",
      "product_quantity": "985",
      "reason_for_recall": "Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to misinterpretation of the optical coherence tomography (OCT) data.",
      "recall_initiation_date": "20150122",
      "center_classification_date": "20150204",
      "termination_date": "20160304",
      "report_date": "20150211",
      "code_info": "Catalog numbers:  000000-20107-750 (DVD with either FORUM v 3.1 or v 3.1.1)  000000-2058-601 (DVD with either FORUM v 3.2 or 3.2.1);  000000-2084-928 (USB drive with FORUM 3.2.1)"
    }
  ]
}