{
  "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": "2026-09-30",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99681",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of Colorado and Florida.",
      "recall_number": "Z-3257-2026",
      "product_description": "Brand Name: VOLARA System  Product Name: VOLARA, HC, NA A  Model/Catalog Number: M08594A  Software Version: N/A  Product Description: VOLARA, HOMECARE, NORTH AMERICA  Component: No",
      "product_quantity": "2",
      "reason_for_recall": "Contamination within the release test equipment flow path could have affected the accuracy of the  nebulizer flow rate. Affected devices returned to firm and testing confirmed devices meet specifications.",
      "recall_initiation_date": "20260803",
      "center_classification_date": "20260923",
      "report_date": "20260930",
      "code_info": "Lot Code: UDI: 00887761981690 Serial Numbers: W078SY3553 and Z309SY7853",
      "more_code_info": ""
    }
  ]
}