{
  "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": [
    {
      "country": "United States",
      "city": "Hudson",
      "address_1": "5 Wentworth Dr",
      "reason_for_recall": "Inner tray label may adhere to wall of outer tray which make it difficult to remove the tray onto the sterile field",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Product manufactured between April 3, 2012 and May 14, 2013 and can be identified by their expiration date; between April 2017 and May 2018.",
      "center_classification_date": "20130930",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and internationally to the following countries:  American Samoa   Antilles  Argentina   Australia   Austria   Bangladesh   Belgium   Bolivia   Brazil   Canada   Chile   Colombia   Egypt   El Salvador   Finland   France   Germany   Great Britain   Greece   Guatemala   Hong Kong   India   Indonesia   Ireland   Italy   Jamaica   Japan   Korea   Lebanon   Libya   Malaysia   Mauritius  Mexico   Neal   New Zealand   Nicaragua   Norway   Pakistan  Panama   Peru   Philippines   Poland   Portugal   Puerto Rico   Romania   Russia   Saudi Arabia   Singapore   Slovenia   South Africa   Spain   Switzerland   Taiwan   Thailand   the Netherlands   Trinidad   Tunisia",
      "state": "NH",
      "product_description": "Flixene IFG Vascular Grafts >or= 6mm  Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.",
      "report_date": "20131009",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Atrium Medical Corporation",
      "recall_number": "Z-2305-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65697",
      "termination_date": "20140715",
      "more_code_info": "",
      "recall_initiation_date": "20130712",
      "postal_code": "03051-4929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}