{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "East Syracuse",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99284",
      "recalling_firm": "Intersurgical Inc",
      "address_1": "5010 Campuswood Dr Ste 102",
      "address_2": "",
      "postal_code": "13057-1561",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of CT, FL, IN, MI, OH & VA.",
      "recall_number": "Z-2953-2026",
      "product_description": "One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.",
      "product_quantity": "1,575 units",
      "reason_for_recall": "Devices could potentially be occluded or partially occluded.",
      "recall_initiation_date": "20260615",
      "center_classification_date": "20260814",
      "report_date": "20260826",
      "code_info": "REF: 1000035; Single Unit UDI: 5030267049844; Case UDI: 05030267044528; Lot No. 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565.",
      "more_code_info": ""
    }
  ]
}