{
  "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": "Columbia",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96649",
      "recalling_firm": "Ambu Inc.",
      "address_1": "6721 Columbia Gateway Dr Ste 200",
      "address_2": "N/A",
      "postal_code": "21046-3380",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, CO, FL, GA, KY, MD, MT, NJ, NV, PA, TN, TX, VA.",
      "recall_number": "Z-1723-2025",
      "product_description": "Ambu aScope\" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US",
      "product_quantity": "160 units",
      "reason_for_recall": "Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.",
      "recall_initiation_date": "20250407",
      "center_classification_date": "20250506",
      "report_date": "20250514",
      "code_info": "Model Number: 622002000US. UDI-DI: 05707480156542. Lot Number: 1001080963",
      "more_code_info": ""
    }
  ]
}