{
  "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": "2026-06-24",
    "results": {
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      "city": "South Jordan",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Merit Medical Systems, Inc.",
      "address_1": "1600 W Merit Pkwy",
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      "postal_code": "84095-2416",
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      "recall_number": "Z-2003-2026",
      "product_description": "Philips Bridge Prep Kit  REF: K12-09098C  Sterile EO, Rx ONLY",
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      "reason_for_recall": "catheter may experience resistance when being advanced over the guidewire",
      "recall_initiation_date": "20260402",
      "center_classification_date": "20260429",
      "report_date": "20260506",
      "code_info": "All Lot Numbers/UDI: 00884450816509",
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