{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94713",
      "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": "Nationwide distribution. International distribution to Canada, France, and Germany.",
      "recall_number": "Z-2322-2024",
      "product_description": "Volara System. Blue Ventilator Adapter Module.  Intermittent positive pressure breathing device component.",
      "product_quantity": "350 units",
      "reason_for_recall": "Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter.  The handset plug is required to ensure proper operation and ventilator gas flow.",
      "recall_initiation_date": "20240530",
      "center_classification_date": "20240717",
      "report_date": "20240724",
      "code_info": "Product Code: M07937; Lot numbers: 4210495, 4325617.",
      "more_code_info": ""
    }
  ]
}