{
  "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": "Hudson",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77342",
      "recalling_firm": "Atrium Medical Corporation",
      "address_1": "5 Wentworth Dr",
      "address_2": "N/A",
      "postal_code": "03051-4929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution-US (nationwide) and countries of: Germany, Great Britain, Austria, Ireland, Netherlands, France, Italy, Sweden, and San Marino.",
      "recall_number": "Z-2761-2017",
      "product_description": "Atrium iCAST Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number  85455 (Marketed in U.S. only)    Atrium Advanta V12 Balloon Expandable Covered Stent; 7mm x 22mm x 120cm;  Model/Part Number  85355 (Marketed OUTSIDE U.S. only)      The iCAST Covered Stent is indicated for the treatment of tracheobronchial strictures produced by malignant neoplasms.",
      "product_quantity": "246 (US: 183 units; Foreign: 63 units)",
      "reason_for_recall": "Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x 22mm x 120cm received an ADVANTA v12 7 mm x 38 mm x 80 cm, due to the manifold (catheter hub) was printed as 7mm x 38 mm x 80 cm. The complaint was the result of incorrect dimensional information (7mm x 38mm x 80cm) printed on the manifiold (catheter hub).  The complaint device physical dimensions matched the dimensional information displayed on the outer packaging and the device inner pouch.  This was the only complaint received for this non-conformance.",
      "recall_initiation_date": "20170525",
      "center_classification_date": "20170725",
      "termination_date": "20200626",
      "report_date": "20170802",
      "code_info": "Part Number 85455: Lots 240735, 240523;   Part Number 85355: Lot 240734"
    }
  ]
}