{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "East Syracuse",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90855",
      "recalling_firm": "Intersurgical Inc",
      "address_1": "6757 Kinne St",
      "address_2": "N/A",
      "postal_code": "13057-1215",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "OH, TN, TX",
      "recall_number": "Z-0096-2023",
      "product_description": "Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg    Model Number: 8003000",
      "product_quantity": "340 pieces",
      "reason_for_recall": "Printing error on the device, size 3 Solus Standard laryngeal mask airway has been incorrectly marked with size 4 information (includes the number 4 as a size identifier, patient weight and maximum inflation volume on the airway tube and the marking #4 on the inflation line pilot balloon) may pose health risk to the patient",
      "recall_initiation_date": "20220829",
      "center_classification_date": "20221017",
      "termination_date": "20231019",
      "report_date": "20221026",
      "code_info": "UDI-DISingle unit: 5030267073511 UDI-DICase: 05030267046959 Lot code: 32204071",
      "more_code_info": ""
    }
  ]
}