{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Elkton",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79167",
      "recalling_firm": "Terumo Medical Corporation",
      "address_1": "950 Elkton Blvd",
      "address_2": "N/A",
      "postal_code": "21921-5322",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "To be added.",
      "recall_number": "Z-0725-2018",
      "product_description": "Destination Guiding Sheath catheter introducer, Catalog Number: RSR06    Product Usage:  The Destination¿ Guiding Sheath is designed to be used for the introduction of interventional and diagnostic devices into the human vasculature, including but not limited to the renal, carotid, and peripheral arteries.",
      "product_quantity": "33",
      "reason_for_recall": "The tucking depth feature of this catheter introducer is marginally outside the upper specification.",
      "recall_initiation_date": "20170912",
      "center_classification_date": "20180226",
      "termination_date": "20180831",
      "report_date": "20180307",
      "code_info": "Lot: VK09, Expiration Date: 31-Jan-2020"
    }
  ]
}