{
  "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": "76138",
      "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": "Nationwide",
      "recall_number": "Z-1221-2017",
      "product_description": "Atrium PVC  8 Fr Straight Thoracic Catheter\t  Code Number: 8008",
      "product_quantity": "660 cases (10/case)",
      "reason_for_recall": "Labeling  icon depicts a catheter having six (6) eyelets; however the correct number of eyelets on the 8 Fr and 10 Fr thoracic catheters is two (2)",
      "recall_initiation_date": "20170120",
      "center_classification_date": "20170216",
      "termination_date": "20201103",
      "report_date": "20170222",
      "code_info": "All Lot Numbers With Expiration Date Prior To December 2019",
      "more_code_info": ""
    }
  ]
}