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FDA (Device enforcement)Recalled 2023-05-19class ii

Baxter Healthcare Corporation: NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed

Hazard

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.

Details from the source

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. Distribution: US Nationwide distribution in the states of OR, SC, VA, TN, GA, NC, CO, NC, FL. Quantity: 7 software versions Lot/code info: 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

UPC codes

00887761985193

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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