Teleflex recalls 62,882 Hudson RCI Sheridan tubes Teleflex is recalling 62,882 Hudson RCI Sheridan Sher-I-Bronch Endobronchial Tubes manufactured from October 2013 to April 2015, according to a notice posted on the FDA's website. Teleflex Medical has received customer complaints about the endobroncial tube's double swivel connector. The connector may break or separate on the tube. If this happens, the device may leak, causing the patient to not receive enough oxygen or experience respiratory distress. This can lead to the need to re-intubate the patient, patient injury or death. The recall is Class I and was initiated on June 1.