{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Redwood City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93320",
      "recalling_firm": "AURIS HEALTH INC",
      "address_1": "150 Shoreline Dr",
      "address_2": "",
      "postal_code": "94065-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution: AK,\tAL,\tAZ,\tCA, CO, CT, DC, DE, FL, GA, IL, IN, KY, MA, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NY, OH, OR, PA, SC, SD, TN, TX, WI & WV.",
      "recall_number": "Z-0448-2024",
      "product_description": "Monarch Platform  REF MON-000005-01, 100-240V- 50/60Hz 1440w",
      "product_quantity": "110 units In total",
      "reason_for_recall": "Their is the potential that software issues  may result in flipped image of the virtual Bronchoscope view.",
      "recall_initiation_date": "20231018",
      "center_classification_date": "20231201",
      "report_date": "20231213",
      "code_info": "Software Version 2.2.4",
      "more_code_info": ""
    }
  ]
}