{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Athlone",
      "state": "N/A",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79643",
      "recalling_firm": "Teleflex Medical Europe Ltd",
      "address_1": "Ida Business Park",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "TX",
      "recall_number": "Z-1628-2018",
      "product_description": "Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical anesthetics to the oropharynx and upper airway region",
      "product_quantity": "25 units",
      "reason_for_recall": "Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.",
      "recall_initiation_date": "20180319",
      "center_classification_date": "20180503",
      "termination_date": "20190827",
      "report_date": "20180509",
      "code_info": "Lot Number 161212"
    }
  ]
}