{
  "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": "2026-07-01",
    "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": "98888",
      "recalling_firm": "Ventec Life Systems, Inc.",
      "address_1": "22002 26th Ave Se",
      "address_2": "N/A",
      "postal_code": "98021-4903",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of UT.",
      "recall_number": "Z-2525-2026",
      "product_description": "VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001",
      "product_quantity": "1",
      "reason_for_recall": "Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.",
      "recall_initiation_date": "20260508",
      "center_classification_date": "20260623",
      "report_date": "20260701",
      "code_info": "REF/UDI-DI/Serial Number/Lot:  PRT-00853-000/00855573007839/155391P/807138, PRT-00490-001/00855573007792/155391/804613"
    }
  ]
}