Navicare Patient Safety; Voalte Patient Safety
Brand(s)
Last updated
Summary
Product
Navicare Patient Safety; Voalte Patient Safety
Issue
Medical devices - Performance issue
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Navicare Patient Safety; Voalte Patient Safety |
Software v.3.9.200 to 4.0.401 |
Not applicable. |
Issue
Baxter Corporation is issuing an urgent medical device correction for the Voalte Patient Safety, previously branded as Navicare Patient Safety, software versions 3.9.200 through 4.0.401. Baxter identified a potential risk where the "safety" monitoring and "bed exit" monitoring features may enter a permanent state of alert suppression.
Recall start date: May 23, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Hill-Rom, Inc.
1225 Crescent Green Drive, Cary, North Carolina, United States, 27518-8119
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73749
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