{
  "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": {
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Miami Lakes",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91922",
      "recalling_firm": "Cordis US Corp",
      "address_1": "14201 Nw 60th Ave",
      "address_2": "N/A",
      "postal_code": "33014-2802",
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      "reason_for_recall": "There is a potential for separation of the ANGIOGUARD  RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement device is prepared.",
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      "center_classification_date": "20230511",
      "report_date": "20230517",
      "code_info": "UDI/DI 20705032053508; Lot Numbers:  35262517, 35263334, 35264204, 35264222, 35265345."
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}