{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Gieres",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84713",
      "recalling_firm": "Blue Ortho",
      "address_1": "6 Allee De Bethleem",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "AZ, CA, FL, TN  Foreign: Italy",
      "recall_number": "Z-1149-2020",
      "product_description": "Blue Ortho TKA Pro v2.1 software installed on the Exactech GPS system -indicated for stereotaxic surgery in Knee Arthroplasty  Catalog Reference: L00002",
      "product_quantity": "7 units",
      "reason_for_recall": "The navigated values displayed when using the LPI instrumentation are incorrect due to software inconsistencies (wrong data loaded).",
      "recall_initiation_date": "20190922",
      "center_classification_date": "20200211",
      "termination_date": "20200723",
      "report_date": "20200219",
      "code_info": "TKA Pro v2.1 software",
      "more_code_info": ""
    }
  ]
}