# Major Recall Alert: Carestation 620, Carestation 650, Carestation 750 A Recalled Due to Unexpected Shutdown of Carestation 600 and 700 Series Anesthesia Systems
The Carestation 620, Carestation 650, and Carestation 750 A anesthesia systems are facing a significant recall in Canada. The issue involves the unexpected shutdown of Carestation 600 and 700 series anesthesia systems containing specific power management boards, which can occur when AC mains power is disconnected or lost. This recall is raising concerns as these systems play a critical role in patient care during medical procedures. Here's what you need to know and how you can protect yourself and affected patients.
## Why This Recall is Important
The recalled Carestation 600 and 700 series anesthesia systems are used widely in medical and surgical settings. These devices are responsible for administering anesthesia and monitoring patients' vital signs during operations. If these systems unexpectedly shut down due to a power issue:
- **Patient safety could be compromised.** An abrupt loss of anesthesia or vital sign monitoring poses serious risks, particularly during complex surgeries.
- **Operational delays may occur.** Hospitals and clinics may face disruptions in their workflow needing immediate alternatives.
- **Legal and regulatory implications** could arise as healthcare providers must ensure patient care aligns with safety standards.
Prompt action is critical to mitigate these risks and ensure patient care remains unaffected.
## Details of the Recall
Here are the key details about the recall:
- **Category:** Unexpected shutdown of Carestation 600 and 700 series anesthesia systems upon AC mains power loss or disconnection
- **Brands Affected:** Carestation 620, Carestation 650, Carestation 750 A
- **Product Models:** Carestation 620, Carestation 650, Carestation 750 A
- **Reason for Recall:** Faulty power management boards in these anesthesia systems, leading to an unexpected shutdown when AC mains power is disconnected or interrupted.
- **Date Announced:** October 2023
- **Official Source:** [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/carestation-600-and-700-series-anesthesia-systems)
If you own or work with these models, reviewing your inventory and taking immediate steps is essential for maintaining patient safety in your facility.
## What You Should Do
To ensure safety and compliance with this recall, follow these critical steps:
- **Inspect Your Equipment:** Verify if your anesthesia systems are among the affected models (Carestation 620, 650, and 750 A).
- **Contact the Manufacturer:** Reach out to the equipment provider or manufacturer to confirm if your device is included in the recall and arrange for repairs or replacements.
- **Use Backup Systems:** In the interim, rely on backup anesthesia systems to prevent disruptions in patient care.
- **Inform the Team:** Notify all relevant staff and departments to ensure everyone is aware of the recall and associated risks.
- **Report Incidents:** If an unexpected shutdown has already occurred, report it to the manufacturer and health authorities.
Your timely response is vital to ensure patient safety and avoid any risks associated with these faulty systems.
## Stay Safe – Get Instant Recall Alerts
Recalls like this one highlight the importance of staying informed and proactive. Keep your team and facility up-to-date with the latest recall alerts to safeguard patient care.
**Download the [My Recalls App](https://myrecalls.app)** now to receive real-time notifications about product recalls, safety issues, and updates directly to your device. Stay one step ahead when it comes to protecting your patients and ensuring compliance with safety regulations.
Don’t wait—act today to address this critical recall and ensure patient safety in your healthcare facility!
For more information about this recall, visit the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/carestation-600-and-700-series-anesthesia-systems).