{
  "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": "Terminated",
      "city": "Paris",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80938",
      "recalling_firm": "EOS Imaging",
      "address_1": "4 Ieme Etage",
      "address_2": "10 Rue Mercoeur",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide",
      "recall_number": "Z-3188-2018",
      "product_description": "sterEOS workstation",
      "product_quantity": "17 units",
      "reason_for_recall": "3D projections may be incorrect when  the pair of images used is a secondary capture generated from a series containing more than two images, where one of the images has been manually flipped.  Projection errors may lead to errors in calculation of 3D clinical parameters when  adjusting the position, size and shape of the 3D objects used.  Incorrect clinical parameters can be a contributing factor in incorrect clinical decisions, or sub-optimal surgical interventions.",
      "recall_initiation_date": "20180801",
      "center_classification_date": "20180918",
      "termination_date": "20220815",
      "report_date": "20180926",
      "code_info": "All software versions are impacted"
    }
  ]
}