{
  "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": "81000",
      "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": "US: CA (Mountain View and San Jose)    A single system.  No distributed OUS.",
      "recall_number": "Z-0108-2019",
      "product_description": "Carl Zeiss Meditec AG, Goeschwitzer Strasse 51-52 07745 Jena, Germany,  IOLMaster 700, REF 1932-169  SN 1185393  2017-09-01",
      "product_quantity": "1",
      "reason_for_recall": "Calibration setting was incorrectly entered during manufacturing causing the optical coherence tomography (OCT) to obtain the incorrect two-dimensional images of ocular structures of the anterior and posterior segments of the eye.",
      "recall_initiation_date": "20180625",
      "center_classification_date": "20181015",
      "termination_date": "20210115",
      "report_date": "20181024",
      "code_info": "Model: 700  Catalog Number: 000000-1932-169  Serial Number: 1185393  UDI: 04049471092080"
    }
  ]
}