{
  "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": "75599",
      "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 the countries of Algeria, Australia, Austria, Belgium, Brazil, Canada, Chile, China, China, Columbia, Ecuador, Egypt, Finland, France, Germany, Great Britain, Greece, Guatemala, Hong Kong, Ireland, Italy, Kuwait, Lebanon, Libya, Mexico, Netherlands, New Zealand, Pakistan, Panama, Peru, Poland, Portugal, Puerto Rico, Saudi Arabia, South Korea, Spain, Sweden, Thailand, Tunisia, and Venezuela,",
      "recall_number": "Z-1082-2017",
      "product_description": "Atrium Medical Ocean Blood Recovery Drains as  follows:  2050-000\tOcean Blood Recovery drain with in-line connector and suction control stopcock   2050-300\tOcean Blood Recovery drain with suction control stopcock, no in-line connector  2052-000\tOcean Double Blood Recovery drain with in-line connector and suction control stopcock - 2 patient lines connected by one \u001cY\u001d connector  2052-300\tOcean Double Blood Recovery drain with suction control stopcock, no in-line connector - 2 patient lines connected by one \u001cY\u001d connector    Product Usage:  To evacuate air and/or fluid from the chest cavity or mediastinum. \u001c To help re-establish lung expansion and restore breathing dynamics. \u001c To facilitate postoperative collection and reinfusion of autologous blood from the patient s pleural cavity or mediastinal area.",
      "product_quantity": "964,463 cases  (US)   521,975 cases (OUS) in total",
      "reason_for_recall": "Outer Packaging is not sterile",
      "recall_initiation_date": "20161129",
      "center_classification_date": "20170124",
      "termination_date": "20200929",
      "report_date": "20170201",
      "code_info": "All Lot Numbers With Expiration Date Prior To  October 2019"
    }
  ]
}