Baxter Healthcare Corporation: Medical Device Recall in 2023 - (Recall #: Z-2007-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed

Product Classification:

Class II

Date Initiated: May 19, 2023

Date Posted: July 5, 2023

Recall Number: Z-2007-2023

Event ID: 92300

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 7 software versions

Code Information:

UDI/DI 00887761985193, Software Versions: 3.9: 3.9.200,3.9.201, 3.9.300, 3.9.400, 3.9.401, 3.9.500, 3.9.600

Distribution Pattern:

US Nationwide distribution in the states of OR, SC, VA, TN, GA, NC, CO, NC, FL.

Voluntary or Mandated:

Voluntary: Firm initiated