{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96286",
      "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": "US Nationwide distribution.",
      "recall_number": "Z-1419-2025",
      "product_description": "Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087",
      "product_quantity": "93 units",
      "reason_for_recall": "There is a software issue which causes the upper back section to not be operable/adjustable when the \"emergency mode\" function is enabled.",
      "recall_initiation_date": "20250225",
      "center_classification_date": "20250321",
      "report_date": "20250402",
      "code_info": "UID/DI 00887761974067, All serial numbers manufactured until 11/14/2024."
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}