{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fremont",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71608",
      "recalling_firm": "EXP Pharmaceutical Services Corp",
      "address_1": "48021Warm Springs Boulevard",
      "address_2": "N/A",
      "postal_code": "94539",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in DC and the states of CO, CA, FL, TX, and AR.",
      "recall_number": "Z-2251-2015",
      "product_description": "Medical Device Exchange  Chocolate Balloon Catheter/Over-the-Wire;  Pouch, Tyvek/Mylar, Sterile, Single Use Only;  OEM Catalog number CF14-150-25040-OTW.  EXP (repackager), TriReme Medical  (OEM)    Catheter, angioplasty, peripheral, transluminal",
      "product_quantity": "1",
      "reason_for_recall": "EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that its vendors were registered and had their own quality systems.",
      "recall_initiation_date": "20150211",
      "center_classification_date": "20150724",
      "termination_date": "20151230",
      "report_date": "20150805",
      "code_info": "OEM Catalog number CF14-150-25040-OTW."
    }
  ]
}