{
  "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": [
    {
      "status": "Terminated",
      "city": "Palm Harbor",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75785",
      "recalling_firm": "Oscor, Inc.",
      "address_1": "3816 Desoto Blvd",
      "address_2": "N/A",
      "postal_code": "34683-1618",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US including CA, NJ, MD, TX, FL, NC, MO, and Puerto Rico.  Internationally to AUSTRIA, BOLIVIA, CANADA, CHILE, CYPRUS, NETHERLANS, EGYPT, GERMANY, HONG KONG, ISRAEL, ITALY, SWITZERLAND, and VIETNAM",
      "recall_number": "Z-0815-2017",
      "product_description": "MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F  C55¿ S79CM D84CM GLOBAL  Catalog # 990079-055-000  Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.",
      "product_quantity": "59",
      "reason_for_recall": "Complaint  that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.",
      "recall_initiation_date": "20161005",
      "center_classification_date": "20161219",
      "termination_date": "20190726",
      "report_date": "20161228",
      "code_info": "Lot #'s: C1-08936 Exp. May 18, 2017 and OR-04635 Exp. March 10, 2018"
    }
  ]
}