{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "South Jordan",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93461",
      "recalling_firm": "Merit Medical Systems, Inc.",
      "address_1": "1600 W Merit Pkwy",
      "address_2": "N/A",
      "postal_code": "84095-2416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AL, AZ, CA, CO, CT, FL, IA, IL, IN, \tKS, MA, MD, MN, MO, NH, NJ, NSW, NV, NY, UT, WI and the countries of Argentina, Australia, Belgium, China, France, Germany, Guam, Hong Kong, Italy, Mexico, Netherlands, Switzerland.",
      "recall_number": "Z-0629-2024",
      "product_description": "Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY",
      "product_quantity": "3 units",
      "reason_for_recall": "The sterility of microcatheter and infusion system devices cannot be guaranteed.",
      "recall_initiation_date": "20231106",
      "center_classification_date": "20240102",
      "report_date": "20240110",
      "code_info": "REF: IS4-135-30  Lot # H2765720 UDI: 00884450000885  REF: IS4-90-10  Lot # H2765603 UDI: 00884450006504"
    }
  ]
}