Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
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Medical Devices Recalls
Medical equipment, implants, and diagnostic devices
37,779 Total Recalls
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
Megadyne Medical Products
Class I - Dangerous
Firm has received reports of patient burns in surgical procedures where device was used.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
DigitalDiagnost C90, Model No. 712034 and 712035
Philips North America
Class I - Dangerous
There is a software login in issue that may prevent the user from logging in.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
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 111781050
TELEFLEX
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Class I - Dangerous
The inner needle of the Sertera device is either detaching or discharging and may cause delay in surgery
Class I - Dangerous
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left
Waldemar Link GmbH & Co. KG (Mfg Site)
Class I - Dangerous
The firm discovered through customer complaints that device segments may not meet specifications.
RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.
Appliedvr
Class I - Dangerous
There is the potential for the program software to malfunction which will not allow it to move forward to the next session.