{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "North Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98106",
      "recalling_firm": "Fresenius Kabi USA, LLC",
      "address_1": "50 High St Ste 50",
      "address_2": "",
      "postal_code": "01845-2620",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, CO, FL, GA, ID, IL, MD, MI, MI, MN, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA, WI, WI.",
      "recall_number": "Z-1048-2026",
      "product_description": "Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.",
      "product_quantity": "30 units",
      "reason_for_recall": "Emphasizing instructions for LVP duration programming located in the IFU.",
      "recall_initiation_date": "20251121",
      "center_classification_date": "20260112",
      "report_date": "20260121",
      "code_info": "Product Code: LVP-SW-0005; UDI: 00811505030122; Software versions 5.10.2 and prior.",
      "more_code_info": ""
    }
  ]
}