All 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.

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.

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

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.

Delay in reporting results due to Quality Controls running high outside of range. Target value and range for ACTH in Immunoassay Premium Level 3, IA2640, lot 2031EC and Immunoassay Premium Control Tri Level kit batch 583135 lot 2031EC has been reassigned on the Roche Cobas e801 due to High recovery outside range

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

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.

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.

The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction.

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

A cardioversion procedure may damage the electronics in the Vanta INS device, making the INS unresponsive and non-functional. As of April 19, 2023, Medtronic has received a total of two complaints concerning this issue from patients implanted with a Vanta INS, both of which have resulted in explant procedures.

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