Teleflex, Inc.: Medical Device Recalls in 2015

According to to data from the FDA, there were 11 medical device recalls made by Teleflex, Inc. in 2015. See the details of the recalls below.

You can see similar recalls for other firms.

• White Bronchial Double Lumen Tube Set (Right) Sterile
• Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
• Bronchial Double Lumen Tube Set (Left), Sterile
• Bronchial Double Lumen Tube Set (Right), Sterile
• Tracheopart Set (Left), Sterile
• Carlens Bronchial Double Lumen Tube Set (Left) Sterile
• Tracheopart Set (Right), Sterile
• Bronchial One Lumen Tube - Right
• Bronchial One Lumen Tube - Left
• R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation.
• MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.