Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Other Medical Devices
🏥 Medical Devices • 15,203 recalls
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075
TELEFLEX
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery
Megadyne Medical Products
Firm has received reports of patient burns in surgical procedures where device was used.
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060
TELEFLEX
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080
TELEFLEX
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
Baxter Healthcare
Baxter identified a potential risk where the "safety" monitoring and "bed exit" monitoring features may enter a permanent state of alert suppression. In this state, a caregiver may not be alerted remotely when assigned patient protocols (bed exit, siderail position, brakes off, height of bed changes, head of bed angle, and/or turn reminders) are turned off.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Voalte Patient Safety, Part Number 4.0, V4.0.000 to 4.0.401, used with the Centrella Bed
Baxter Healthcare
Baxter identified a potential risk where the "safety" monitoring and "bed exit" monitoring features may enter a permanent state of alert suppression. In this state, a caregiver may not be alerted remotely when assigned patient protocols (bed exit, siderail position, brakes off, height of bed changes, head of bed angle, and/or turn reminders) are turned off.