Voalte Nurse Call System provides a comprehensive communication and information system that places patient calls, sta
Summary
The FDA issued a Class II for Voalte Nurse Call System provides a comprehensive communication and informati by Baxter Healthcare Corporation. Reason: Firm discovered a firmware memory leak with a supplier-manufactured component..
Details
Source
Device Recall
External ID
Z-1094-2022
Action Date
2022-05-25
Status
Terminated
Category
device
Product Description
Voalte Nurse Call System provides a comprehensive communication and information system that places patient calls, staff calls, and emergency calls.
Lot/Code Info: Internal Part Number: 4.0.; UDI/GTIN: 00887761995079; P2519NNC3A24 model number of impacted RubyTech Switch
Quantity Affected: 1414 units
Reason for Recall
Firm discovered a firmware memory leak with a supplier-manufactured component.
Distribution
US Distribution to states of: NC and VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-13
Company
Deerfield, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 164 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Baxter Healthcare Corporation has 310 FDA actions in our database, including 286 recalls and 24 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Baxter Healthcare Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Baxter Healthcare Corporation have FDA actions?
Baxter Healthcare Corporation has 310 FDA actions in our database, including 286 recalls and 24 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1094-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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