{
  "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": "2026-04-01",
    "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": "88388",
      "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": "US Nationwide Distribution - AR, OH, SC, WA, PA, WI, IA, and FL",
      "recall_number": "Z-2385-2021",
      "product_description": "DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.5MM SOLID, 145 CM, REF DBP-150SOLID145",
      "product_quantity": "8 units",
      "reason_for_recall": "There is a potential mislabeling of the OAD crown sizes:  1.50mm Sold Crown OADs may be packaged s 1.25mm Micro Crown OADs and vice versa.",
      "recall_initiation_date": "20210721",
      "center_classification_date": "20210828",
      "termination_date": "20260318",
      "report_date": "20210908",
      "code_info": "Lot 340925"
    }
  ]
}