{
  "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": "95929",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.",
      "recall_number": "Z-1009-2025",
      "product_description": "Baxter Solution Set with Duo-Vent Spike, REF 2R8404",
      "product_quantity": "",
      "reason_for_recall": "Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.",
      "recall_initiation_date": "20241220",
      "center_classification_date": "20250122",
      "report_date": "20250129",
      "code_info": "UDI/DI 00085412676630, Lot Numbers:  DR24C22079 (exp.3/247/2026), DR24H23086 (exp. 8/26/2026)",
      "more_code_info": ""
    }
  ]
}