{
  "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": "Santa Rosa",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66532",
      "recalling_firm": "Medtronic Vascular, Inc.",
      "address_1": "3576 Unocal Pl",
      "address_2": "N/A",
      "postal_code": "95403-1774",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-0154-2014",
      "product_description": "Resolute Integrity Zotarolimus-eluting Coronary Stent:  Stent ID 3.0 mm; Stent length 34 mm; Rx, Sterile.  Mfg in Medtronic Ireland, Galaway, Ireland. Distributed by: Medtronic Inc.  Minneapolis, MN.    Indicated for improving coronary luminal diameters in patients.",
      "product_quantity": "201 units",
      "reason_for_recall": "A small number of units in lot number 0006573585 of the Resolute Integrity Zotarolimus-Eluting Coronary Sten System may contain a compliance chart incorrectly referencing a 2.25 mm diameter instead of the correct 3.0mm.",
      "recall_initiation_date": "20131007",
      "center_classification_date": "20131105",
      "termination_date": "20140211",
      "report_date": "20131113",
      "code_info": "Model: RSINT30034UX;   Customer Facing Number: RSIST30034UX.  Expiration date: 25 May 2014."
    }
  ]
}