{
  "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": "2026-10-28",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bothell",
      "state": "WA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99835",
      "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": "Distribution US nationwide including Puerto Rico.",
      "recall_number": "Z-0126-2027",
      "product_description": "VOCSN   Model Number: PRT-01100-000, Package PN:PRT-01126-000. used for ventilatory support.",
      "product_quantity": "1,532 units",
      "reason_for_recall": "Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.",
      "recall_initiation_date": "20260917",
      "center_classification_date": "20261020",
      "report_date": "20261028",
      "code_info": "All Serial Numbers: UDI: 00855573007747",
      "more_code_info": ""
    }
  ]
}