{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "204473",
      "product_res_number": "Z-0564-2024",
      "event_date_initiated": "2023-11-17",
      "event_date_posted": "2023-12-15",
      "recall_status": "Open, Classified",
      "res_event_number": "93475",
      "product_code": "MRN",
      "product_description": "VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at the point of use",
      "code_info": "Lot Code: W-0001-2023, Cassette serial numbers:  GA01T707, GA01T108",
      "firm_fei_number": "3014617112",
      "recalling_firm": "Vero Biotech, LLC",
      "address_1": "387 Technology Cir Nw Ste 125 387 Technology Cir Nw",
      "address_2": "Ste 125",
      "city": "Atlanta",
      "state": "GA",
      "postal_code": "30313-2411",
      "additional_info_contact": "908-388-3980",
      "reason_for_recall": "Cassette did not meet an 1n-process flow criterion.",
      "root_cause_description": "Process control",
      "action": "VERO BIOTECH issued an URGENT:  MEDICAL DEVICE REMOVAL notice to its consignees on 11/17/2023 via email,  The notice explained the issue and advised the consignee of the removal of the device from their possession on 11/03/2023.",
      "product_quantity": "2 cassettes",
      "distribution_pattern": "US:  AZ and FL",
      "openfda": {
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        "device_name": "Apparatus, Nitric Oxide Delivery",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5165",
        "device_class": "2",
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