{
  "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": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98180",
      "recalling_firm": "VANTIVE US HEALTHCARE LLC",
      "address_1": "510 Lake Cook Rd",
      "address_2": "N/A",
      "postal_code": "60015-4964",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1230-2026",
      "product_description": "PRISMAFLEX HF1000 SET, Product Code 107142; Dialyzer, High Permeability With Or Without Sealed Dialysate System",
      "product_quantity": "115,112 units",
      "reason_for_recall": "There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.",
      "recall_initiation_date": "20260106",
      "center_classification_date": "20260202",
      "report_date": "20260211",
      "code_info": "UDI/DI 07332414069315, All lots including and manufactured after 24F0094CA"
    }
  ]
}