{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86062",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution throughout the United States, St. Thomas USVI, and Puerto Rico.  Foreign distribution including Canada, Caribbean (Barbados, Trinidad and Tobago, Jamaica, Bahamas, Bermuda, and Guyana)",
      "recall_number": "Z-0123-2021",
      "product_description": "Spectrum IQ Infusion System with Dose IQ Safety Software",
      "product_quantity": "146,224 units",
      "reason_for_recall": "Baxter is updating the device IFU for safety communication regarding cleaning practices.",
      "recall_initiation_date": "20200630",
      "center_classification_date": "20201022",
      "termination_date": "20240429",
      "report_date": "20201028",
      "code_info": "Product Code: 3570009, All Serial Numbers; GTIN 00085412610900"
    }
  ]
}