🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
All Recalls
95,094 total recalls in our database
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
A comingle/swap resulted in the labeling and laser marking on the product to state it is a Aequalis Flex Revive Assembly Screw 0mm Standard (ARS655101) but it was a Aequalis Flex Revive Assembly Screw 0mm Short (ARS655118) & vice versa.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
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 111780080
TELEFLEX
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery
Megadyne Medical Products
🏥 Medical Devices Class I - Dangerous
Firm has received reports of patient burns in surgical procedures where device was used.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
A software bug affecting results when using deep learning (DL) segmentation followed by geometrical functions: Create wall function, Expand Contract function or ROI algebra function, the results are incorrect. If dose statistics for an incorrectly created ROI are used to determine if a plan is acceptable for treatment, this could potentially lead to an inappropriate plan being approved. The error could lead to a more conservative or more liberal plan than intended.
🏥 Medical Devices Class I - Dangerous
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 111780055
TELEFLEX
🏥 Medical Devices Class I - Dangerous
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 111780090
TELEFLEX
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
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 111780035
TELEFLEX
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
🏥 Medical Devices Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.