{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "New Taipei City",
      "state": "N/A",
      "country": "Taiwan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81009",
      "recalling_firm": "Besmed Health Business Corporation",
      "address_1": "No.5, Lane 116, Wu-Kong 2nd Road",
      "address_2": "Wu-Ku District",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide, and country of Canada.",
      "recall_number": "Z-0109-2019",
      "product_description": "Ambu Aura40 Standard, Reusable Laryngeal Mask  Catalog Number: 340300000",
      "product_quantity": "267 units",
      "reason_for_recall": "Ambu Aura40 Standard, Reusable Laryngeal Mask  packaged in a pouch marked AuraStraight Silicone, Single Use Laryngeal Mask   Sterile",
      "recall_initiation_date": "20180809",
      "center_classification_date": "20181015",
      "termination_date": "20190510",
      "report_date": "20181024",
      "code_info": "Lot Numbers: MO0612G40021 and MO0605G40014"
    }
  ]
}