{
  "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": "Fremont",
      "address_1": "5055 Brandin Ct",
      "reason_for_recall": "The incorrect outer carton box was used for the product.",
      "address_2": "",
      "product_quantity": "3 catheters",
      "code_info": "AngioSculpt PTCA lot #G18090030.",
      "center_classification_date": "20191126",
      "distribution_pattern": "Distribution was made to IA, MI, and NJ.  There was government distribution.  There was no military/foreign distribution.",
      "state": "CA",
      "product_description": "Spectranetics AngioSculpt PTCA Scoring Balloon Catheter, balloon outer diameter 2.5mm, balloon length 15mm, REF 2027-2515, Sterile, Rx.  The firm name on the label is Spectranetics Corporation, Fremont, CA.",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Spectranetics Corporation",
      "recall_number": "Z-0576-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84057",
      "termination_date": "20201027",
      "more_code_info": "",
      "recall_initiation_date": "20181207",
      "postal_code": "94538-3140",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}