{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "37368",
      "product_res_number": "Z-0681-05",
      "event_date_initiated": "2005-02-23",
      "event_date_posted": "2005-04-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-07-31",
      "res_event_number": "31205",
      "product_code": "CBI",
      "k_numbers": [
        "K851856"
      ],
      "product_description": "Sheridan Sher-I-Bronch  Endobronchial Tube for Right Bronchial Intubation; an Rx, sterile, sinlge use endobronchial tube with modified tip for right bronchial intubation, 37 Fr.; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-16137",
      "code_info": "catalog number  (REF) 5-16137, lot numbers 1148460 and 1147062",
      "firm_fei_number": "3004959265",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2345 Waukegan Rd",
      "address_2": "Suite 120",
      "city": "Bannockburn",
      "state": "IL",
      "postal_code": "60015",
      "additional_info_contact": "Ms. Julie McDowell\n610-948-2836",
      "reason_for_recall": "The distal end of the tube may be printed incorrectly, with catalog numbers V5-16037 and 5-16037 stating 'Bronchial - Right' instead of 'Bronchial - Left', and catalog number 5-16137 stating 'Bronchial - Left' instead of 'Bronchial - Right'.",
      "root_cause_description": "Other",
      "action": "Customers were notified via Federal Express, Next Business Day Delivery, on February 23, 2005.  The accounts were informed of the mislabeling and were  instructed to inspect the product lots for any incorrectly printed devices, comparing the writing on the sleeve of the blue bronchial tube with the package label which is correct, and to return all identified affected product to Teleflex Medical, Hudson RCI.",
      "distribution_pattern": "Nationwide and internationally to Argentina, Canada, Chile, China, Costa Rica, Hong Kong, Korea, the Netherlands, South Africa and Vietnam.",
      "openfda": {
        "k_number": [
          "K251950",
          "K897046",
          "K894337",
          "K120334",
          "K051522",
          "K232529",
          "K083883",
          "K160542",
          "K181886",
          "K071694",
          "K111522",
          "K203749",
          "K121462",
          "K002288",
          "K113576",
          "K200968",
          "K953483",
          "K201026",
          "K925615",
          "K152251",
          "K123853",
          "K093888",
          "K010596",
          "K013865",
          "K222340",
          "K021920",
          "K851856",
          "K141888",
          "K253096",
          "K962167",
          "K232580",
          "K180253",
          "K092886",
          "K961977"
        ],
        "registration_number": [
          "2011171",
          "3004040397",
          "3014656749",
          "3018094310",
          "3009093866",
          "2032112",
          "3013023209",
          "3003898360",
          "8040412",
          "3004111573",
          "2936999",
          "3013528571",
          "3010400865",
          "3005609751",
          "3010220595",
          "9681384",
          "1423662",
          "2025816",
          "1000563940",
          "3009171251",
          "9610691",
          "3010131137",
          "3012050423",
          "3000308637",
          "9617604",
          "1314417",
          "3004784537",
          "3004748541",
          "3011137372",
          "3006425876",
          "3006017180",
          "3006984712",
          "1820334",
          "3007134520",
          "3007797756",
          "3014766734"
        ],
        "fei_number": [
          "2011171",
          "3005747797",
          "3003076831",
          "3004040397",
          "3014656749",
          "3002558692",
          "3018094310",
          "3002807626",
          "3009093866",
          "3013023209",
          "3003898360",
          "3004111573",
          "3006759904",
          "2936999",
          "3010400865",
          "3013528571",
          "3010220595",
          "3009271244",
          "3005609751",
          "2025816",
          "1000563940",
          "3010131137",
          "3012050423",
          "3000308637",
          "1314417",
          "3000215273",
          "3002806359",
          "3004784537",
          "3004748541",
          "3006425876",
          "3006017180",
          "3006984712",
          "1820334",
          "3007134520",
          "3007797756",
          "3014766734"
        ],
        "device_name": "Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5740",
        "device_class": "2"
      }
    }
  ]
}