{
  "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": "2026-04-22",
    "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": "66222",
      "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": "Nationwide distribution.",
      "recall_number": "Z-0109-2014",
      "product_description": "Vented Spike Adapter Product Code 2C0471, Sterile, nopyrogenic. Manufactured by an affiliate of Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield IL 60015 USA.    An IV transfer device, used to transfer fluids in pharmacy compounding system.",
      "product_quantity": "49,344 units",
      "reason_for_recall": "Potential tears in the pouch of six lots of Vented Spike Adapter Product Code 2C0471",
      "recall_initiation_date": "20130830",
      "center_classification_date": "20131029",
      "termination_date": "20170419",
      "report_date": "20131106",
      "code_info": "R13D09024, R13D09107, R13D12101, R13D17068, R13D18066, R13D20070"
    }
  ]
}