{
  "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": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64158",
      "recalling_firm": "Codman & Shurtleff, Inc.",
      "address_1": "325 Paramount Drive",
      "address_2": "N/A",
      "postal_code": "02767",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Austria, Belgium, Canada, Chile, Costa, Rica, Czech Republic, Denmark, France, Germany, Great Britian/UK, Ireland, Italy, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovakia, Spain, and Switzerland.",
      "recall_number": "Z-0863-2013",
      "product_description": "NEUROPATH 6Fx90 GUIDING CATH S2  Product Code: GSM60900000    Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices",
      "product_quantity": "64 units",
      "reason_for_recall": "Sterility of device may be compromised due to lack of package integrity",
      "recall_initiation_date": "20130111",
      "center_classification_date": "20130220",
      "termination_date": "20150810",
      "report_date": "20130227",
      "code_info": "All unexpired lots"
    }
  ]
}