# Major Recall Alert: BD Alaris™ Pump Module Faces Issues That Could Lead to Serious Health Risks
If you use the BD Alaris™ Pump Module, it's essential to be aware of a critical product recall that could impact its performance. BD (Becton, Dickinson, and Company) has announced a recall following reports that dropping the device or exposing it to severe jarring can lead to hidden internal damage. This damage may interfere with the pump module’s proper operation, resulting in severe risks like under-infusion, over-infusion, unregulated flow, or calibration failure.
BD Alaris™ Pump Modules play a vital role in patient care, so understanding the recall details and taking appropriate action is crucial. Keep reading to learn everything you need to know about this recall and how to safeguard your health.
## Why This Recall is Important
The BD Alaris™ Pump Module recall is significant due to the critical role these devices play in healthcare settings. These infusion pumps are responsible for delivering precise medication doses to patients. When the internal components are damaged, even minor flaws can have catastrophic consequences.
Here’s why this recall requires immediate attention:
- **Hidden Internal Damage**: Impacts like drops or severe jarring may not show visible damage, making it challenging to identify problems early.
- **Serious Health Risks**: Malfunctions from internal damage may cause:
- **Under-infusion**, where patients receive less medication than needed.
- **Over-infusion**, leading to overdose risks.
- **Unregulated flow**, potentially introducing hazards like toxicity.
- **Calibration failure**, forcing the module to operate improperly or not at all.
Patient safety is a top priority, and BD’s recall highlights the critical need to address these potential issues immediately.
## Details of the Recall
Here are the key facts concerning the BD Alaris™ Pump Module recall:
- **Affected Product**: BD Alaris™ Pump Module.
- **Recall Reason**: Internal components may sustain unnoticed damage due to drops or rough handling. This damage compromises the bezel assembly, which is critical for ensuring accurate pumping.
- **Potential Risks**: Damage may cause under-infusion, over-infusion, unregulated flow, or calibration failure, all of which could jeopardize patient safety.
- **Date Announced**: Noted on October 2023.
- **Official Source for Details**: For more information, visit the official recall notice on the [Government of Canada’s website](https://recalls-rappels.canada.ca/en/alert-recall/bd-alaristm-pump-module).
It’s imperative for healthcare providers and individuals to take this recall seriously, given the far-reaching consequences of a malfunctioning device in clinical or personal care settings.
## What You Should Do
If you own or use the BD Alaris™ Pump Module, take the following steps:
1. **Inspect Devices**: Check your pump module for any signs of damage. Even if none are visible, consider replacing or servicing the device.
2. **Follow Manufacturer Instructions**: Refer to BD's official guidance for handling and using these devices to minimize the risk of damage.
3. **Contact BD**: Reach out to BD’s support team for more information on what to do next.
4. **Report Problems**: If you experience any issues, file a complaint with Health Canada or BD to report the malfunction.
Do not take risks with your safety or the safety of others—proactively addressing this recall is essential.
## Stay Safe – Get Instant Recall Alerts
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### Learn More
To review the full recall details for the BD Alaris™ Pump Module, visit the official recall notice from the Government of Canada [here](https://recalls-rappels.canada.ca/en/alert-recall/bd-alaristm-pump-module).
Stay safe and ensure your devices are functioning properly!