{
  "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": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78897",
      "recalling_firm": "Cardiovascular Systems Inc",
      "address_1": "1225 Old Highway 8 NW",
      "address_2": "N/A",
      "postal_code": "55112-6416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, IL, MI, MN, MO, NY, SC, TX, and WI",
      "recall_number": "Z-0505-2018",
      "product_description": "Peripheral Diamondback 1.25 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in patients with occlusive atherosclerotic disease in peripheral arteries and who are acceptable candidates for percutaneous transluminal atherectomy.",
      "product_quantity": "8",
      "reason_for_recall": "Cardiovascular Systems, Inc. (CSI) is removing the products because it was identified that the labeling for two lots of product s were potentially inadvertently switched during production.",
      "recall_initiation_date": "20170914",
      "center_classification_date": "20180202",
      "termination_date": "20191104",
      "report_date": "20180214",
      "code_info": "Lot # 190097  Part #: 7-10012  Model # DBP-125SOLID145"
    }
  ]
}