{
  "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": "66400",
      "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": "US Distribution including the states of CO, VA, and MS.",
      "recall_number": "Z-0045-2014",
      "product_description": "Merit Medical Performa Angiographic Catheter 5F Multipack.  Part numbers 7560-43 and 7560-G3.",
      "product_quantity": "200",
      "reason_for_recall": "4 lots of Performa Cardiac Multipacks contain a JR4.0 catheter with a slight variation in tip shape.",
      "recall_initiation_date": "20130913",
      "center_classification_date": "20131022",
      "termination_date": "20140103",
      "report_date": "20131030",
      "code_info": "Part Number/Lot Number: 7560-43/I663860, 7560-43/I663861, 7560-G3/I664519 and 7560-G3/I666388."
    }
  ]
}