# Major Recall Alert: Novum IQ LVP Recalled Due to Software Anomalies Causing Blank Run Screens
Baxter Corporation has issued an urgent medical device correction for its **Novum IQ Large Volume Pump (LVP)**. The recall, which began on **August 7, 2025**, stems from software anomalies that could cause a blank run screen during operation – a critical issue for healthcare providers and patients relying on the device.
If you or your healthcare facility uses the Novum IQ LVP, it's crucial to be aware of this correction and take steps to mitigate potential risks. Here's everything you need to know, including what you should do to stay safe.
## Why This Recall is Important
The **Novum IQ Large Volume Pump (LVP)** is commonly used in healthcare environments to deliver fluids, medications, and nutrients to patients with precision. However, the identified **software anomalies** may result in the screen on the pump going blank during operation. This malfunction could:
- Delay essential treatment.
- Lead to errors in administering fluids or medications.
- Pose serious risks to patient safety.
While no injuries tied to this issue have been publicly reported yet, it's essential to address this problem immediately to prevent potential harm. Baxter Corporation is working closely with healthcare providers and regulatory authorities to resolve the issue and update all affected devices.
## Details of the Recall
Key information about the recall includes:
- **Brand**: Novum IQ LVP
- **Product Name**: Large Volume Pump (LVP)
- **Reason for Recall**: Software anomalies result in a blank run screen during operation.
- **Recall Start Date**: August 7, 2025
- **Image of Product**: 
The recall involves a correction of the software issue identified in the pump. Baxter Corporation has advised healthcare facilities and providers to follow precautionary instructions to minimize associated risks until the software fix has been implemented.
For further details, check the **official recall notice here**: [Government of Canada Recall Notice: Novum IQ LVP](https://recalls-rappels.canada.ca/en/alert-recall/novum-iq-lvp-4).
## What You Should Do
If your facility uses the **Novum IQ LVP**, take the following actions immediately to ensure patient safety:
- **Follow Baxter's Guidance**: Adhere to the urgent medical device correction instructions issued by Baxter Corporation.
- **Inspect Devices**: Carefully check all Novum IQ LVP devices and ensure users are aware of the potential issue with the run screen.
- **Update Software**: Contact Baxter Corporation or authorized service personnel to schedule the software update.
- **Monitor Patients Closely**: Until the correction is applied, closely monitor patients to prevent delays or errors caused by a device malfunction.
Healthcare providers with concerns or questions are urged to contact Baxter Corporation directly for additional support and resources.
## Stay Safe – Get Instant Recall Alerts
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Stay informed, stay safe, and help spread the word about the **Novum IQ LVP recall** to ensure patient safety across Canada!