{
  "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": "2026-04-08",
    "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": "78570",
      "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": "Letter",
      "distribution_pattern": "Nationwide Distribution to AZ, CA, GA, IA, IL, KY, MA, NC, NE, SC, TN, VA",
      "recall_number": "Z-0188-2018",
      "product_description": "Everflex Self-Expanding Peripheral Stent with Entrust Delivery System   Intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 140 mm in length in the native Superficial Femoral Artery (SFA) and/or proximal popliteal arteries with reference vessel diameters ranging from 4.5 - 7.5 mm.",
      "product_quantity": "21 units",
      "reason_for_recall": "Stent length on the label may not match the length of the stent itself.",
      "recall_initiation_date": "20171103",
      "center_classification_date": "20171129",
      "termination_date": "20200901",
      "report_date": "20171206",
      "code_info": "Model No. EVD35-07-060-120, UDI 00821684051436, Lot No. A476328.      Model No. EVD35-07-120-120, UDI 00821684051467, Lot No. A476301."
    }
  ]
}