Reported Jul 5, 2023 · Ongoing
NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
- Lot codes and dates
- UDI/DI 00887761985193
- Software Versions
3.9: 3.9.2003.9.2013.9.3003.9.4003.9.4013.9.5003.9.600
- Amount recalled
- 7 software versions
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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