{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Saint Paul",
      "address_1": "1225 Old Hwy 8 NW",
      "reason_for_recall": "The pouch label was missing the use by date (UBD) of 2018-04.",
      "address_2": "",
      "product_quantity": "190 units (38 - 5 pack shelf cartons)",
      "code_info": "Lot #160877, UDI Number: (01)10852528005084(17)180430(10)160877.",
      "center_classification_date": "20160627",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "MN",
      "product_description": "ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box.  For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and Diamondback 360.  Cardiovascular.",
      "report_date": "20160706",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cardiovascular Systems Inc",
      "recall_number": "Z-2051-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74445",
      "termination_date": "20160816",
      "more_code_info": "",
      "recall_initiation_date": "20160613",
      "postal_code": "55112-6416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}