{
  "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": "Completed",
      "city": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82525",
      "recalling_firm": "Medtronic Vascular",
      "address_1": "35 Cherry Hill Dr # 37a",
      "address_2": "N/A",
      "postal_code": "01923-2565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution to US, Austria, Belgium, Bulgaria, Czech Republic, France, Germany, Greece, Hong Kong, Ireland, Italy, Kazakhstan, Luxembourg, Moldova, Netherlands, Poland, Portugal, Russian Federation, Saudi Arabia, Slovakia, South Africa, Spain, Sweden, Taiwan, and United Kingdom",
      "recall_number": "Z-2648-2019",
      "product_description": "SHERPA NX ACTIVE GUIDING CATHETER, 6F JL6.0, .070\",  REF SA6JL60.   for cardiovascular use",
      "product_quantity": "136 units",
      "reason_for_recall": "There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.",
      "recall_initiation_date": "20190315",
      "center_classification_date": "20190930",
      "termination_date": "20240426",
      "report_date": "20191009",
      "code_info": "GTIN: 00613994822437  All Lot/Serial Numbers"
    }
  ]
}