{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Somerset",
      "address_1": "2101 Cottontail Ln",
      "reason_for_recall": "During recent routine testing, the MISAGO Peripheral Stent was found not to conform to product specification related to stent diameter at the proximal/distal ends and/or the shape of the stent.",
      "address_2": "",
      "product_quantity": "7,965 units",
      "code_info": "150401 150429 150713 150821 150923 151009 160314    150413 150501 150708 150824 150915 151013 151111    150415 150515 150701 150716 150902 151005 151106    150407 150514 150707 150827 151008 151109 160509    150406 150501 150713 150716 150825 151001 151102 160315 160509  150410 150710 150831 150909 151007 151012 151014 151103 151208  150417 150429 150717 150910 151002 151102 160510    150408 150429 150701 150717 150831 151013 151103 160512   150409 150430 150518 150703 150706 150903 150914 151005   150331 150430 150708 150714 150904 150910 151001 151102   150414 150429 150715 150903 151005 151029 160323    150416 150518 150715 150908 150915 151002 151106 160328   150401 150430 150716 150828 151006      150403 150514 150717 150901 150909 151012     150408 150430 150713 150907 151001      150402 150512 150713 150907 151001",
      "center_classification_date": "20161129",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "MISAGO RX Self Expanding Peripheral Stem",
      "report_date": "20161207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Terumo Medical Corp",
      "recall_number": "Z-0669-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75370",
      "termination_date": "20171019",
      "more_code_info": "",
      "recall_initiation_date": "20160804",
      "postal_code": "08873-1277",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}