{
  "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": "St Martin D Heres",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87391",
      "recalling_firm": "Imactis",
      "address_1": "20 Rue Du Tour De L Eau",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "NJ, NY, WI",
      "recall_number": "Z-1264-2021",
      "product_description": "Impactis NaviKit-stereotaxic accessory for Computed Tomography systems    Reference # I10100",
      "product_quantity": "105 kits",
      "reason_for_recall": "Defect in the mechanical assembly of the needle holder contained in the navigation kit. One of the 2 jaws of the needle holder does not provide gripping functionality; if the defect is not detected before use, it can cause poor needle guidance and a lack of precision during navigation causing an inaccurate needle position which could cause damage to organs or vasculature adjacent to the trajectory",
      "recall_initiation_date": "20210211",
      "center_classification_date": "20210316",
      "termination_date": "20231005",
      "report_date": "20210324",
      "code_info": "Lots #: 20060001, 20060005  UDI-DI: B681I101002"
    }
  ]
}