{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95842",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US, Nationwide Distribution",
      "recall_number": "Z-0887-2025",
      "product_description": "Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP",
      "product_quantity": "1 unit",
      "reason_for_recall": "There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.",
      "recall_initiation_date": "20241220",
      "center_classification_date": "20250116",
      "report_date": "20250122",
      "code_info": "UDI/DI 00887761978089 or 00815410020537, Serial Numbers:  122010001081",
      "more_code_info": ""
    }
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}