{
  "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": "75707",
      "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 Internationally to Canada and Mexico",
      "recall_number": "Z-1205-2017",
      "product_description": "Maquet Ocean Water Seal Chest Drain, Single Collection WAC  Reference: 2002-000    Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. \" To help re-establish lung expansion and restore breathing dynamics. \" To facilitate postoperative collection and reinfusion of autologous blood from the patients pleural cavity or mediastinal area.",
      "product_quantity": "245 cases (1470 units)",
      "reason_for_recall": "Chest drains manual vent valve located at the top of affected chest drains could potentially not re-seal after being depressed.",
      "recall_initiation_date": "20161223",
      "center_classification_date": "20170215",
      "termination_date": "20201103",
      "report_date": "20170222",
      "code_info": "Lot Number: 242896, 243292",
      "more_code_info": ""
    }
  ]
}