Teleflex Medical Europe Ltd FDA Recalls

4 recalls on file across devices, 0 of them Class I and 0 still open. Matched by name to TFX.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d) 1Class IIJul 16, 2021The firm received reports that the endotracheal tube cuff co	The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained f	Class IIDevices	Jul 16, 2021
RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 504550 b) 504555 c) 504560 dClass IIJul 16, 2021The firm received reports that the endotracheal tube cuff co	The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained f	Class IIDevices	Jul 16, 2021
RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 Class IIJul 16, 2021The firm received reports that the endotracheal tube cuff co	The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained f	Class IIDevices	Jul 16, 2021
RUSCH Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF numbers: a) 112080050 b) 112080055 c)Class IIJul 16, 2021The firm received reports that the endotracheal tube cuff co	The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained f	Class IIDevices	Jul 16, 2021