All Recalls

There is the potential for the program software to malfunction which will not allow it to move forward to the next session.

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.

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.

Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.

Reagent lot numbers include an insufficient concentration of blocking reagent.

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

The firm discovered through customer complaints that device segments may not meet specifications.

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

There is a software login in issue that may prevent the user from logging in.

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Firm has received reports of patient burns in surgical procedures where device was used.

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

The firm discovered through customer complaints that device segments may not meet specifications.

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit (Part No. 20-005-022) and the VERIGENE Enteric Pathogens Nucleic Acid Test Kit (Part No. 20-005-023) could provide a false-negative result due to hydrophobic characteristics in specific FLOQSwab lots.