{
  "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": "Bothell",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99660",
      "recalling_firm": "Ventec Life Systems, Inc.",
      "address_1": "22002 26th Ave Se",
      "address_2": "",
      "postal_code": "98021-4903",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of FL, IA, OH, NE, TN.",
      "recall_number": "Z-3222-2026",
      "product_description": "REF:HF2PC9  HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver",
      "product_quantity": "2 units",
      "reason_for_recall": "Labeling; Oxygen Cylinders do not contain required medical gas labeling",
      "recall_initiation_date": "20260728",
      "center_classification_date": "20260918",
      "report_date": "20260930",
      "code_info": "UDI:00850018761352/Serial #s:  24IKMA0029J and 24IKMA002CM",
      "more_code_info": ""
    }
  ]
}