# Major Recall Alert: Impella® Controller Recalled Due to Detection Issue Impacting Pump Functionality
Abiomed, a leading name in medical technology, has announced a critical recall for its Automated Impella Controller™ (AIC). The issue, which affects Impella® pumps during specific conditions, could impair the detection of the pump when connected to the controller. This detection failure could occur during a console-to-console transfer or at the start of a case, without any visual alarm appearing on the AIC screen to alert users. This recall began on July 7, 2025, and addresses a serious safety concern for patients relying on the use of this advanced medical device.
Read below for all the details and tips on how to protect yourself and your loved ones.
## Why This Recall is Important
The Abiomed Impella® Controller is an essential tool designed to manage Impella® heart pumps, which provide advanced cardiac support in critical care settings. However, the identified issue poses serious risks:
- **Pump Mismanagement Risk**: A failure to detect the Impella® pump could delay appropriate care or lead to operational failure.
- **No Visual Alarm**: The absence of a visible alert exacerbates the problem, leaving medical professionals unaware of the issue.
- **Widespread Impact**: This problem could occur with **any Abiomed Impella® pump**.
Given the importance of the Impella® pump in life-saving procedures, this malfunction poses a significant threat to patient health and safety. Addressing this recall immediately is critical for hospitals, healthcare providers, and affected users.
## Details of the Recall
Here’s an overview of the Abiomed Impella® Controller recall:
- **Product Name**: Automated Impella Controller™ (AIC)
- **Brand**: Impella® Controller
- **Issue**: Pump detection impairment during console-to-console transfer or case start, with **no visible alarm system** to indicate the problem.
- **Recall Start Date**: **July 7, 2025**
- **Devices Affected**: Virtually any Abiomed Impella® pump reliant on the controller could encounter this issue.
For more information, refer to the official recall notice on the [Government of Canada's Recall and Safety Alerts website](https://recalls-rappels.canada.ca/en/alert-recall/impellar-controller).
## What You Should Do
If you use or oversee the operation of Impella® Controllers, it’s essential to follow these safety measures:
1. **Contact Abiomed Support Immediately**: Reach out to Abiomed customer service to confirm whether your device is affected and discuss next steps.
2. **Follow Updated Safety Procedures**: Abiomed may provide guidance to mitigate risks or replace malfunctioning devices.
3. **Monitor Your Device**: Ensure enhanced vigilance during console transfers and case starts, as these are key moments when detection failure may occur.
4. **Stay Informed**: Keep track of updates related to this recall and ensure all staff are trained on proper handling.
By taking these steps, you can safeguard patients from potential harm associated with the Impella® Controller malfunction.
## Stay Safe – Get Instant Recall Alerts
In today’s fast-paced world, staying informed about product recalls is vital, especially for critical medical devices like the Abiomed Impella® pumps. Don’t wait to hear about product issues – download our **recall alert app** today for real-time notifications that could save time and lives.
- **Benefits**:
- Instant push notifications for recalls in your area
- Device-specific alerts tailored to your needs
- Stay ahead of potential safety risks
[Click here](https://recalls-rappels.canada.ca/en/alert-recall/impellar-controller) to learn more about this recall, and don’t forget to download the recall alert app to keep you and your loved ones informed and protected.
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This recall serves as a critical reminder of the importance of vigilance in the medical field. Ensuring the functionality of life-saving devices like the Impella® Controller is essential for improving patient care and outcomes. Stay proactive, stay informed, and stay safe.