{
  "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": [
    {
      "country": "United States",
      "city": "Grand Rapids",
      "address_1": "2680 Walker Ave Nw",
      "reason_for_recall": "The device was built with the rigid insertion stylet instead of the flexible stylet.",
      "address_2": "",
      "product_quantity": "35 units",
      "code_info": "Lot code: 00794-030718",
      "center_classification_date": "20181004",
      "distribution_pattern": "US Distribution to state of:  SC.",
      "state": "MI",
      "product_description": "Retrograde Cardioplegia Cannula, Model Number RMG-0015S     The Retrograde Cardioplegia Cannula is intended for use in perfusing cardioplegia solutions retrograde through the coronary sinus by means of transatrial introduction.",
      "report_date": "20181010",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Surge Medical Sales, LLC (DBA Surge Cardiovascular)",
      "recall_number": "Z-0068-2019",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "81042",
      "termination_date": "20190404",
      "more_code_info": "",
      "recall_initiation_date": "20180718",
      "postal_code": "49544-1385",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}