{
  "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": "E. Syracuse",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76945",
      "recalling_firm": "Intersurgical Inc",
      "address_1": "6757 Kinne St.",
      "address_2": "N/A",
      "postal_code": "13057",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution to the states of :  IL, KY, OH, NY & VA and to the countries of : Canada & Mexico",
      "recall_number": "Z-0208-2018",
      "product_description": "Solus Flexible wire-reinforced laryngeal mask airways under the following sizes:  1) small pediatric size 2 catalog #8002001, 2) large pediatric size 2.5 catalog #8025001, 3) small adult size 3 catalog #8003001, 4) medium adult size 4 catalog #8004001 and 5) large adult size 5 catalog #8005001    Patent airway management.",
      "product_quantity": "144 cases / 20 units",
      "reason_for_recall": "A defect in the wire-reinforced tubing may result in a partial of total occlusion when the cuff is over-inflated.",
      "recall_initiation_date": "20170403",
      "center_classification_date": "20171207",
      "termination_date": "20190617",
      "report_date": "20171213",
      "code_info": "Product Lots: 31402822 to 31610791",
      "more_code_info": ""
    }
  ]
}