{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "LA CIOTAT",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93049",
      "recalling_firm": "OLEA MEDICAL",
      "address_1": "93 AVANUE DU SORBIER,",
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      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-0122-2024",
      "product_description": "Functional MR V1.0",
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      "reason_for_recall": "When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic resonance software bug may cause file contents and associated series descriptions to not match, which could lead to a misinterpretation of clinical data.",
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      "center_classification_date": "20231018",
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}