{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Columbia",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92886",
      "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": "Visit",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-2628-2023",
      "product_description": "Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, portable endoscopy system.    Catalog No: 405011000",
      "product_quantity": "2689 units",
      "reason_for_recall": "Multiple impacts, for example from being dropped, can cause to the Ambu aView 2 Advance to short-circuit and under special circumstances make the lithium-ion battery in the device combust leading to smoke and flames",
      "recall_initiation_date": "20230721",
      "center_classification_date": "20230922",
      "report_date": "20231004",
      "code_info": "UDI: 5707480145089  Version no.: 054 thru 056; 058 thru 059 Product manufactured prior to Oct 29, 2020"
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}