{
  "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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    }
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  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85405",
      "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 only to Puerto Rico and Guam",
      "recall_number": "Z-2066-2020",
      "product_description": "Prismaflex Control Unit",
      "product_quantity": "5 devices US territories",
      "reason_for_recall": "Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.",
      "recall_initiation_date": "20200407",
      "center_classification_date": "20200521",
      "termination_date": "20211109",
      "report_date": "20200527",
      "code_info": "Product Code: 114870; Lot Number: PA18198, PA18199, PA18238, PA22556, PA22558."
    }
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}