# Major Recall Alert: CentriMag™ Adult ECMO Kit, CentriMag™ Blood Pump Recalled Over Safety Notification
**Attention healthcare professionals:** Abbott has issued a voluntary recall customer notification for its **CentriMag™ Acute Circulatory Support System**, including the **CentriMag™ Adult ECMO Kit** and **CentriMag™ Blood Pump**. This recall is not a product removal but serves as a critical reminder to always ensure the **CentriMag™ blood pump is securely locked into the CentriMag™ motor**, as outlined in the **instructions for use (IFU)**. Improper locking of the pump could lead to **particulate generation** or **increased heat** during use, posing a potential safety concern.
When the pump is securely locked into the motor, the system functions as intended and remains safe for patient use. Here's what healthcare providers need to know.
## Why This Recall Is Important
The CentriMag™ Acute Circulatory Support System is widely used for critical care, including procedures like extracorporeal membrane oxygenation (ECMO). Proper operation of this system is vital for patient safety.
Abbott's voluntary recall customer notification highlights a potential issue:
- **Improper locking of the blood pump into the motor** can lead to safety risks, such as:
- **Particulate generation**
- **Increased motor heat**
- If left unaddressed, these issues could compromise the system's reliability during use.
This recall is not requesting a product return or removal but instead warns users to **closely follow the IFU guidelines** to ensure proper operation. When used correctly, the product is safe and effective.
## Details of the Recall
Here are the critical details you need to know concerning this recall notice:
- **Brand Affected:** CentriMag™
- **Products Involved:**
- CentriMag™ Adult ECMO Kit
- CentriMag™ Blood Pump
- **Recall Reason:** Reminder to securely lock the CentriMag™ blood pump into the motor, per the IFU, to prevent safety risks.
- **Action Required:** No products need to be returned or removed from the field. However, users must review and adhere to the IFU for proper locking procedures.
- **Date Announced:** [Insert date here when accurately determined, as placeholder date 30352 is listed]
- **Source Information:** For the official Health Canada recall announcement, visit [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/centrimagtm-adult-ecmo-kit-and-blood-pump).
Abbott emphasizes that as long as the pump is properly secured, the product continues to be safe and functional.
## What You Should Do
If you're using the CentriMag™ Acute Circulatory Support System, follow these steps immediately:
1. **Review the Instructions for Use (IFU):** Pay close attention to the procedure for securely locking the blood pump into the motor.
2. **Inspect Your Device:** Ensure the pump is properly seated and locked into the motor before each use.
3. **Monitor for Issues:** Stay vigilant for signs of particulate formation or increased heat during operation.
4. **Contact Abbott if Necessary:** If you encounter any issues or have questions, reach out to Abbott for technical support.
Following these guidelines will ensure the continued safety and effectiveness of the CentriMag™ system for your patients.
## Stay Safe – Get Instant Recall Alerts
Patient safety is paramount, and staying informed about recalls like this is essential for healthcare providers. Don’t miss critical updates—download the [MyRecalls App](https://www.myrecalls.app) today to receive instant alerts for product recalls that matter to you. It's free, easy to use, and ensures you're always updated on the latest safety information.
For further details about this recall, visit the official Canadian government recall database: [Health Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/centrimagtm-adult-ecmo-kit-and-blood-pump).
**Stay informed and stay safe!**