{
  "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": {
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      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Maquet Cardiovascular, LLC",
      "address_1": "45 Barbour Pond Dr",
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      "postal_code": "07470-2094",
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      "recall_number": "Z-1337-2023",
      "product_description": "VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W",
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      "reason_for_recall": "Some batches of product were not sterilized to their minimum sterilization specification.",
      "recall_initiation_date": "20230306",
      "center_classification_date": "20230404",
      "report_date": "20230412",
      "code_info": "UDI-DI: 00607567700345; Lot Numbers: 3000274687",
      "more_code_info": ""
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}