FDA (Devices) recall action 71727
The FDA (Devices) publishes a recall like this one as 9 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 9 pages.
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
The agency’s own wording, quoted from the enforcement report.
Teleflex is recalling specific batches of Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling Bronchial One Lumen Tubes - Left because customer complaints reported the cobb connector detaching from the main connector prior to use.
Teleflex is recalling sterile Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling specific lots of Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex, Inc. is recalling White Bronchial Double Lumen Tube Sets (Right) Sterile because the cobb connector may detach from the main connector prior to use.
Teleflex is recalling Carlens Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling Bronchial One Lumen Tubes because the cobb connector may detach from the main connector prior to use.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.