{
  "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": "South Jordan",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73630",
      "recalling_firm": "Merit Medical Systems, Inc.",
      "address_1": "1600 West Merit Parkway",
      "address_2": "N/A",
      "postal_code": "84095",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to one customer in the US.",
      "recall_number": "Z-1375-2016",
      "product_description": "Boston Scientific TSX Transseptal Needle, Model Number M004TSX60o;  Used to create the primary puncture in the interatrial septum when passing an intruder and/or catheter through the septum from the right side of the heart to the left side.",
      "product_quantity": "25",
      "reason_for_recall": "Merit Medical Systems, Inc. is voluntarily conducting a recall of one lot of the TSX\" Transseptal Needle due to a discrepancy between the labeling and the actual configuration of the device in the packaging.  The curve dimensional values on the labels of this lot incorrectly indicate a 50¿ curve, rather than the correct 86¿ curve",
      "recall_initiation_date": "20160315",
      "center_classification_date": "20160412",
      "termination_date": "20160822",
      "report_date": "20160420",
      "code_info": "Lot Q823423, Exp 7/31/2018",
      "more_code_info": ""
    }
  ]
}