Official recall record
NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-05-19
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00887761985193
- Brand on record
- Baxter Healthcare Corporation
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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All 48 official recall notices naming Baxter Healthcare Corporation on this site →
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