{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 3
    }
  },
  "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-3223-2026",
      "product_description": "REF: HF2POSTD  HomeFill Oxygen System  HomeFill cylinder D with CGA870 Compatible Post Valve",
      "product_quantity": "25 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:00850018761376/ Serial #s: 25EKMA00BAC 25EKMA009L3 25EKMA009CM 25EKMA009J8 25GKMA00077 25GKMA0007B 25GKMA0009Z 25GKMA0004U 25GKMA000CS 25GKMA000CR 25GKMA000CX 25GKMA000D0 25GKMA000LL 25GKMA000N1 25GKMA000UD 25GKMA000D1 25GKMA000TN 25GKMA000D2 25GKMA000UC 25GKMA000LK 25GKMA000UA 25GKMA000UB 25GKMA000UE 25GKMA000CY 25GKMA000UF",
      "more_code_info": ""
    }
  ]
}