{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Keene",
      "state": "NH",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67991",
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "address_1": "10 Bowman Dr",
      "address_2": "N/A",
      "postal_code": "03431-5043",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution in the state of North Carolina.",
      "recall_number": "Z-1641-2014",
      "product_description": "Portex Low Dead Space Connector with Sideport, 3.5mm    Product Usage:  The connector is used to attach the endotracheal tube to the patient breathing circuit. The low dead space connector minimizes mechanical dead space and subsequent carbon dioxide rebreathing. The connector's sideport permits access for administration of artificial surfactant, airway pressure monitoring, gas sampling, and instillation of sterile saline for airway leakage.",
      "product_quantity": "100 devices",
      "reason_for_recall": "One lot of 3.0mm sized Connectors, Product Reorder No. 10035-05PS, Lot No. 2553426 were placed in packages labeled as size 3.5mm.",
      "recall_initiation_date": "20140410",
      "center_classification_date": "20140611",
      "termination_date": "20161129",
      "report_date": "20140618",
      "code_info": "Lot or Serial  No:  2553426"
    }
  ]
}