{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72787",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution and the country of Canada",
      "recall_number": "Z-0607-2016",
      "product_description": "Baxter CLEARLINK System, Blood Bag Spike Adapter, Luer Activated Valve for I.C. Access, 1C8687,     Product Usage:  C8687: An accessory to transfer a medicinal product from one container to another container.",
      "product_quantity": "77,136 units",
      "reason_for_recall": "Potential for dark loose particulate matter (400 microns or smaller) on the spike of the spike adapter or solution set.",
      "recall_initiation_date": "20151130",
      "center_classification_date": "20160106",
      "termination_date": "20161030",
      "report_date": "20160113",
      "code_info": "Lot Numbers:  GR323907, GR324806, GR326116, GR326645, GR327528, and GR328534"
    }
  ]
}