{
  "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": "2026-07-01",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Marne La Vallee Cedex 2",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92206",
      "recalling_firm": "Trophy SAS",
      "address_1": "Trophy Sas",
      "address_2": "Trophy; Croissy Beaubourg; 4 Rue Pelloutier",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution",
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      "product_quantity": "895 units",
      "reason_for_recall": "Device failed to function as intended and/or failed to conform to their design specifications.",
      "recall_initiation_date": "20210721",
      "center_classification_date": "20230526",
      "report_date": "20230607",
      "code_info": "CS 9600"
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