The Magazine for Sleep Professionals
Thursday, April 30, 2026
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death Recalled Product Airway Kit containing Sheridan® Endotracheal Tubes Model numbers: Kit TC7855 Distribution Dates: November 28, 2018 to June 5, 2019 Devices Recalled in […]
Teleflex Incorporated has announced a worldwide recall of certain lots of Hudson RCI® Sheridan® Endotracheal Tubes. The recalled products are designed for oral or nasal intubation and are indicated for airway management. The products involved in this recall are as follows: The U.S. Food and Drug Administration (FDA) has classified […]
On September 5, 2017, Smiths Medical ASD issued a voluntary recall of 71 lots of Sterile Water and Saline for Inhalation USP Products (described in further detail below) that either lacked sufficient documentation to assure sterility or may have been susceptible to leaking. Sterile Water for Inhalation USP (350 mLand 550 mL Humidifier with […]
