# Major Recall Alert: Agilia VP MV WiFi CA Infusion Pump Recalled Due to Unjustified Air Alarms
Medical device recalls can have a significant impact on patient safety, and the latest recall involving the **Agilia VP MV WiFi CA Infusion Pump** is no exception. For pumps updated to software versions 4.2 and 4.3, users have reported an increase in air alarms, which were determined to be unjustified. While software version 4.3 is not licensed in Canada, this issue has led to a precautionary recall initiated on **July 16, 2025**. Keep reading for all the details and steps you need to ensure patient safety.
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## Why This Recall is Important
The Agilia VP MV WiFi CA Infusion Pump is a critical device used in healthcare to deliver precise amounts of fluids, medication, or nutrients to patients. A malfunction in such devices poses serious risks.
- **Issue Identified**: Users of software versions 4.2 and 4.3 observed an **unexpected increase in air alarms**, which are essential alerts for detecting air in the infusion line.
- **Problem**: These alarms were judged to be **unjustified**, potentially causing unnecessary interruptions in treatment.
- **Impact on Canada**: While **software version 4.3** is not licensed or deployed in Canada, version 4.2 is in circulation, warranting the recall.
This recall is crucial to ensure that the infusion pumps function without causing undue delays or interruptions in patient care due to false alarms.
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## Details of the Recall
Here are the key facts you need to know about the recall:
- **Product Name**: Agilia VP MV WiFi CA Infusion Pump
- **Brand**: Agilia
- **Recall Start Date**: July 16, 2025
- **Reason for Recall**: Increased reports of unjustified air alarms in pumps updated to software versions 4.2 and 4.3.
- **Impact on Canadian Distribution**:
- Version 4.3 software is **not licensed in Canada** and has not been deployed.
- However, version 4.2 is in use, prompting necessary safety precautions.
For more details, visit the **[official recall notice here](https://recalls-rappels.canada.ca/en/alert-recall/agilia-vp-mv-wifi-ca-infusion-pump)**.
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## What You Should Do
If you or your facility uses the Agilia VP MV WiFi CA Infusion Pump, follow these steps immediately:
1. **Identify Software Version**: Check if your infusion pump is running software version 4.2.
2. **Stop Using Affected Devices**: Discontinue the use of pumps with software version 4.2 until further notice.
3. **Contact Manufacturer**: Reach out to the distributor or manufacturer for guidance on updates or replacements.
4. **Report Issues**: If you’ve experienced problems with the pump, report them to Health Canada or your relevant health authority.
Safety should always be prioritized, particularly in critical medical applications.
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## Stay Safe – Get Instant Recall Alerts
Recalls like this highlight the importance of staying informed about product safety updates. Don’t wait for issues to arise—get notified instantly about recalls that matter to you.
Download the **MyRecalls App** to receive real-time notifications on product recalls across categories, ensuring your safety and that of your loved ones. Be proactive about protecting what matters most!
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For healthcare professionals and patients alike, the **Agilia VP MV WiFi CA Infusion Pump recall** underlines the importance of robust safety standards in medical equipment. Stay informed, act quickly, and prioritize safety to minimize risks from faulty devices.
For the official recall details, visit Health Canada’s website: **[Click here to learn more](https://recalls-rappels.canada.ca/en/alert-recall/agilia-vp-mv-wifi-ca-infusion-pump)**.