{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90730",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1653-2022",
      "product_description": "Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403.  An in-line injection site.",
      "product_quantity": "511,728 units",
      "reason_for_recall": "Firm noted an increase in customer reports of leaks.",
      "recall_initiation_date": "20220809",
      "center_classification_date": "20220909",
      "termination_date": "20240809",
      "report_date": "20220921",
      "code_info": "UDI/DI 00085412656649, All lots within expiry",
      "more_code_info": ""
    }
  ]
}