{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Santa Rosa",
      "address_1": "3576 Unocal Pl",
      "reason_for_recall": "Compliance chart included in lot 207002011 of the NC Sprinter RX 2.25 x 12 mm products lists the size of the device as 2.5mm instead of the correct 2.25mm size.",
      "address_2": "",
      "product_quantity": "122",
      "code_info": "Lot number 207002011;  Exp 5-13-2015.",
      "center_classification_date": "20130930",
      "distribution_pattern": "Worldwide Distribution - USA and the countries of  Australia, Belgium, Canada, Hong Kong, Malaysia, New Zealand, Singapore, Spain, Switzerland, Taiwan and Thailand.",
      "state": "CA",
      "product_description": "NC Sprinter; Rapid Exchange Balloon Dilatation Catheter;  Sterile; 2.25 mm; Model NCSP22512X.  Manufacturer: Medtronic, Inc. 710 Medtronic Parkway Minneapolis, MN 55432    The NC Sprinter Rapid Exchange Balloon Dilatation Catheter is a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid Exchange System. The balloon at the distal end of the catheter can be inflated to a defined diameter at a specific pressure (see labelling). The proximal end of the catheter has a female luer for attachment to an inflation device. The catheter provides a lumen which enables the use of a guide wire to position the catheter. Radiopaque balloon marker(s) enable accurate placement. Shaft markers for brachial and femoral techniques are in place.",
      "report_date": "20131009",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Vascular, Inc.",
      "recall_number": "Z-2302-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66334",
      "termination_date": "20140210",
      "more_code_info": "",
      "recall_initiation_date": "20130916",
      "postal_code": "95403-1774",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}