{
  "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 I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95525",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution (US Nationwide distribution)",
      "recall_number": "Z-0373-2025",
      "product_description": "Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp,  Part Number 5C4482; use in Peritoneal Dialysis",
      "product_quantity": "2,706,558 units",
      "reason_for_recall": "Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like  (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain  peritoneal dialysis and hemodialysis devices.",
      "recall_initiation_date": "20241021",
      "center_classification_date": "20241120",
      "report_date": "20241127",
      "code_info": "UDI/DI 00085412007731, Lot/Serial Numbers: All lots including and manufactured after H19I26088"
    }
  ]
}