{
  "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": "2026-04-01",
    "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": "83527",
      "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": "Letter",
      "distribution_pattern": "US Nationwide",
      "recall_number": "Z-0787-2020",
      "product_description": "Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000.  Airway connector.",
      "product_quantity": "50,400 pieces",
      "reason_for_recall": "The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.",
      "recall_initiation_date": "20190807",
      "center_classification_date": "20200108",
      "termination_date": "20201215",
      "report_date": "20200115",
      "code_info": "Lot numbers:    2182536, 2182852, 2183161, 2190350, 2190531, 2190617, 2191025, 2191591"
    }
  ]
}