# Major Recall Alert: Alaris™ Pump Module & BD Alaris™ Pump Module Recalled Due to Safety Concerns
On **July 16, 2025**, a significant recall was issued for **Alaris™ Pump Modules** and **BD Alaris™ Pump Modules** due to ongoing safety concerns. The issue involves previously recalled bezel kit assemblies, which, despite warnings, are still being used to service these devices. Manufactured between **April 2011 and June 2017** using **fr-110 resin**, these bezel kits can fail, leading to potentially life-threatening risks such as **free flow, over infusion, under infusion, or interrupted infusions**.
Keep reading to understand the details, why this recall is critical, and how you can stay safe.
## Why This Recall is Important
The Alaris™ and BD Alaris™ Pump Modules are essential medical devices widely used in healthcare settings to provide critical infusions of medications and fluids. The safety risks posed by the **recalled bezel kit assemblies** cannot be overstated.
Customer complaints highlighted incidents where these faulty components caused **separated and/or broken bezel bosses** during use. This defect can result in:
- **Free flow of medication**, delivering uncontrolled doses to patients.
- **Over infusion or under infusion**, disrupting accurate medication delivery.
- **Interruption of infusion**, potentially causing delays in critical therapy.
These failures create severe health risks for patients, especially in scenarios requiring precise infusion delivery. It is crucial that healthcare facilities, third-party vendors, and users immediately cease using these defective parts to prevent harm.
## Details of the Recall
Here is a quick summary of the recall details:
- **Products Affected**: Alaris™ Pump Module and BD Alaris™ Pump Module
- **Reason for Recall**: Use of previously recalled bezel kit assemblies made with **fr-110 resin** between April 2011 – June 2017, which may result in defective components.
- **Date of Recall Announcement**: July 16, 2025
- **Key Risks**: Free flow, over infusion, under infusion, or interruption of infusion.
For more details, visit the official recall page: [Canadian Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/alaristm-pump-module-bd-alaristm-pump-module).
## What You Should Do
If you own or work with Alaris™ or BD Alaris™ Pump Modules, take these steps immediately:
- **Cease Usage**: Stop using any bezel kit assemblies manufactured between **April 2011 and June 2017**.
- **Inspect Devices**: Check your pump modules for signs of failure, specifically separated or broken bezel bosses.
- **Contact BD**: Notify BD or your device provider for further instructions on repairs or replacements.
- **Report Issues**: Submit any adverse events or product performance issues to Health Canada or your local health authority.
Prompt action can safeguard patient safety and maintain compliance with regulatory standards.
## Stay Safe – Get Instant Recall Alerts
To avoid risks and stay informed about product recalls like this one, ensure you’re equipped with the tools to act quickly. Download our **free recall alert app** today and receive real-time updates on recalls for medical devices, consumer products, and more.
### Act Now to Protect Patients and Ensure Compliance!
By staying vigilant and informed, we can work together to prevent incidents and safeguard health. For further information, visit the official recall notice [here](https://recalls-rappels.canada.ca/en/alert-recall/alaristm-pump-module-bd-alaristm-pump-module).
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