{
  "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": "2026-04-29",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "Baxter Healthcare Corporation issued an Urgent Device Correction for the SIGMA SPECTRUM Infusion Pump with Master Drug Drug Library due to reports of upstream occlusion alarms and air-in-line alarms occurring during infusions.",
      "address_2": "",
      "product_quantity": "273,835 units",
      "code_info": "Product Code: 35700BAX, 35700ABB  Serial Numbers: All",
      "center_classification_date": "20131108",
      "distribution_pattern": "Worldwide Distribution-USA including Puerto Rico and Canada.",
      "state": "IL",
      "product_description": "SIGMA SPECTRUM Infusion Pump with Master Drug Library.    Intended to be used for the controlled administration of intravenous fluids.",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-0197-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66120",
      "termination_date": "20170420",
      "more_code_info": "",
      "recall_initiation_date": "20130610",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}