{
  "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": "Research Triangle Park",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77980",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2917 Weck Dr",
      "address_2": "N/A",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution",
      "recall_number": "Z-3212-2017",
      "product_description": "LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c)   MAD720 MADgic   Intended for the application of topical anesthetics to the oropharynx and upper airway region",
      "product_quantity": "135,456 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": "20170705",
      "center_classification_date": "20170926",
      "termination_date": "20181120",
      "report_date": "20171004",
      "code_info": "Lot Numbers:  (a) MAD600 MADgic: 161217, 161218, 161228  (b) MAD700 MADgic: 161119, 161120, 161121, 161153, 161173, 161212, 161223, 161236  (c) MAD720 MADgic: 161154"
    }
  ]
}