# Major Recall Alert: Welch Allyn Connex Spot Monitors & Electrocardiographs Recalled Due to Battery Fire Risk
Baxter Corporation has issued an **urgent medical device correction** for several Welch Allyn products, including the Connex Spot Monitor Accessory Power Management Stand (APM), Connex Spot Monitor, Welch Allyn Connex Vital Signs Monitor (CVSM), and Welch Allyn CP150 Electrocardiograph. The recall stems from **battery-related fire hazards** caused by the use of unapproved, third-party batteries. The recall officially began on **March 19, 2025**, and includes critical updates to product manuals outlining the need to use only Baxter-approved batteries.
## Why This Recall is Important
This recall raises severe safety concerns due to incidents of **battery fires** traced back to unauthorized, third-party replacement batteries. Customers who use aftermarket batteries risk **serious property damage and personal injuries**. To prevent further issues, Baxter Corporation is not only warning customers but is also updating the **Instructions for Use (IFUs)** and **service manuals** to reiterate the importance of using Baxter-approved batteries exclusively.
Medical professionals, patients, and institutions that rely on these devices for essential health monitoring must take immediate action to comply with the recall and review the updated guidelines.
## Details of the Recall
Here’s a breakdown of the key information:
- **Products Impacted**:
- Welch Allyn Connex Spot Monitor Accessory Power Management Stand (APM)
- Welch Allyn Connex Spot Monitor
- Welch Allyn Connex Vital Signs Monitor (CVSM)
- Welch Allyn CP150 Electrocardiograph
- **Reason for Recall**:
- **Battery fires** associated with third-party, aftermarket batteries (not approved by Baxter).
- **Action Taken by Baxter Corporation**:
- Updates to IFUs and service manuals.
- Highlighting the dangers of using unapproved batteries.
- **Recall Start Date**: March 19, 2025
For the official announcement, visit [Recalls and Safety Alerts Canada](https://recalls-rappels.canada.ca/en/alert-recall/welch-allyn-connex-vital-signs-monitor-and-electrocardiograph).
## What You Should Do
If you own or use any of the affected devices, take the following steps:
1. **Stop Using Third-Party Batteries**: Immediately discontinue use of third-party, aftermarket batteries.
2. **Replace with Baxter-Approved Batteries**: Use only Baxter-approved replacement batteries to ensure compliance and safety.
3. **Refer to Updated Manuals**: Contact Baxter Corporation for access to updated IFUs and service manuals that include instructions on proper battery use.
4. **Contact Baxter Corporation or Your Supplier**: For further details, assistance, and replacement options.
Healthcare providers and facilities are advised to notify staff and patients about the risks associated with unapproved batteries and implement these changes immediately.
## Stay Safe – Get Instant Recall Alerts
Safety should always come first, especially with critical medical devices. Don’t miss important recall announcements! Stay informed and protect your health by downloading our **free recall alert app**. With real-time notifications and comprehensive product details, you’ll always be up to date on product recalls in Canada.
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For more information on this recall, visit the official source: [Government of Canada Recalls and Safety Alerts](https://recalls-rappels.canada.ca/en/alert-recall/welch-allyn-connex-vital-signs-monitor-and-electrocardiograph).
Stay informed and safe—ensure your devices meet safety standards today! Don’t delay taking action.