{
  "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": "Hudson",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75347",
      "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 -- USA, Australia, Austria, Belgium, Canada, Costa Rica, Dominican Republic, Ecuador, Finland, France, Germany, Honduras, Hong Kong, Ireland, Jamaica, Kuwait, Mexico, Netherlands, New Zealand, Panama, Peru, Portugal, Puerto Rico, Qatar, Reunion, Romania, Saudi Arabia,   South Africa, Spain, Sweden, Switzerland, and Venezuela.",
      "recall_number": "Z-0583-2017",
      "product_description": "Atrium Medical 32 Fr Trocar catheter, Sterile  Model Number:   8432    Intended to facilitate the evacuation of air and/or fluid from the chest cavity or mediastinum.",
      "product_quantity": "5055 cases (10/cs)",
      "reason_for_recall": "Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.",
      "recall_initiation_date": "20161026",
      "center_classification_date": "20161116",
      "termination_date": "20181009",
      "report_date": "20161123",
      "code_info": "All lot codes"
    }
  ]
}