{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87638",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "4600 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-2890",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of NC, CO, CA, AZ, MT, MO.",
      "recall_number": "Z-1532-2021",
      "product_description": "Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.",
      "product_quantity": "23 devices",
      "reason_for_recall": "Incorrect size printed on the device; packaging is labeled correctly.",
      "recall_initiation_date": "20210316",
      "center_classification_date": "20210505",
      "termination_date": "20240415",
      "report_date": "20210512",
      "code_info": "UDI 00643169796348, Lot Number B086915"
    }
  ]
}