{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73706",
      "recalling_firm": "ev3, Inc.",
      "address_1": "3033 Campus Drive",
      "address_2": "N/A",
      "postal_code": "55441",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: CA, GA, LA, MI, MS, MO,NV,NH. NY, OH, PA, SD, TX.    OUS: SINGAPORE",
      "recall_number": "Z-1552-2016",
      "product_description": "ev3, PowerCross\" 0.018\" OTW PTA Dilatation Catheter, model: AB18W030200150, Sterile EO, Rx Only.",
      "product_quantity": "27 (25 US, 2 OUS)",
      "reason_for_recall": "Medtronic is conducting a voluntary Urgent Medical Device Recall of two lots of the PowerCross 0.018\" ¿ Over the Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter because the product is mislabeled.",
      "recall_initiation_date": "20160329",
      "center_classification_date": "20160422",
      "termination_date": "20170519",
      "report_date": "20160504",
      "code_info": "A213373 and A216702"
    }
  ]
}