NaviCare Patient Safety V3.9.200 to 3.9.600 recall
NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
Why was NaviCare Patient Safety V3.9.200 to 3.9.600 recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 7 software versions
- Distribution
- US Nationwide distribution in the states of OR, SC, VA, TN, GA, NC, CO, NC, FL.
- Recall date
- July 5, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)