{
  "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": "Product that was previously recalled because the Chest Drain tubing of the ATS Blood recovery may leak or disconnect, was released for distribution in error.",
      "address_2": "",
      "product_quantity": "195 Cases; Total 1170 units",
      "code_info": "Lot Number: 10906458",
      "center_classification_date": "20140701",
      "distribution_pattern": "Distributed in the states of AK, CA, MD, MN, MO, NC, NJ, OH, and UT.",
      "state": "NH",
      "product_description": "Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N.    Autotransfusion Apparatus.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Atrium Medical Corporation",
      "recall_number": "Z-1959-2014",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "68398",
      "termination_date": "20160317",
      "more_code_info": "",
      "recall_initiation_date": "20140428",
      "postal_code": "03051-4929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}