# Major Recall Alert: CADD-Solis Ambulatory Infusion Pump Recalled Due to Communication Issues with Wireless Module
The CADD-Solis Ambulatory Infusion Pump has been recalled, raising concerns about its safety and functionality in healthcare settings. The issue stems from these pumps losing communication with their wireless communication module due to incompatible hospital network settings. This defect can trigger a high-priority "wireless module intermittent connection" alarm, immediately halting ongoing infusions—a critical issue for patients relying on medication delivery through these devices. The recall began on **April 8, 2025**, and affects healthcare facilities using CADD-Solis pumps across Canada.
If your facility is using the **CADD-Solis Ambulatory Infusion Pump**, here’s what you need to know and do to ensure patient safety.
## Why This Recall is Important
A recall of this nature poses significant risks in inpatient care environments. When the CADD-Solis wireless communication module fails to maintain a connection with the hospital's network, an active alarm stops medication infusion without warning. Infusion interruptions, especially for high-risk or life-saving medications, could severely harm vulnerable patients.
Healthcare networks and settings frequently adjust and upgrade wireless network configurations, which might inadvertently create incompatibility with devices reliant on seamless wireless connectivity. As these pumps are widely utilized for ambulatory infusions, this communication breakdown could jeopardize patient health and safety.
Understanding this recall is imperative to safeguard patients and mitigate risks in clinical environments.
## Details of the Recall
Here are the key points about the **CADD-Solis Ambulatory Infusion Pump** recall:
- **Brand**: CADD-Solis Ambulatory Infusion Pump
- **Product**: CADD-Solis Ambulatory Infusion Pump
- **Recall Reason**: Wireless network configuration issues may cause the device to lose communication with its wireless module, resulting in a high-priority alarm halting medication infusion.
- **Recall Start Date**: April 8, 2025
- **Image of Affected Product**:
- **Official Announcement**: [Government of Canada Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/cadd-solis-ambulatory-infusion-pump)
## What You Should Do
If you are a healthcare provider or facility manager utilizing the **CADD-Solis Ambulatory Infusion Pump**, take these steps immediately:
- **Check Affected Devices**: Identify all CADD-Solis pumps in use to confirm if they are impacted.
- **Consult Wireless Network Settings**: Ensure that your hospital's current network configuration is compatible with the **CADD wireless communication module**. Seek technical support to minimize disruptions.
- **Follow Safety Protocols**: If a malfunction occurs, replace or manually monitor infusion pumps to prevent interruption in medication delivery.
- **Contact the Manufacturer**: Reach out to **CADD-Solis support** to discuss corrective actions or software updates to resolve compatibility issues.
Act swiftly to prevent patient harm and comply with updated guidance from health regulators.
## Stay Safe – Get Instant Recall Alerts
Safety in healthcare starts with staying informed. The recall of the **CADD-Solis Ambulatory Infusion Pump** highlights the importance of being proactive with device updates and recalls. Don’t risk missing critical product alerts—stay ahead of potential risks by getting real-time information on device recalls.
**Download the [Recall App](https://recalls-rappels.canada.ca/en/alert-recall/cadd-solis-ambulatory-infusion-pump) today** and receive instant notifications about recalls in Canada. Whether you’re a healthcare provider, patient, or caregiver, this tool can help ensure product safety without compromise.
**Protect your patients—act now!**
Staying aware and taking proactive steps is the best way to manage recalls effectively. Visit the [official recall webpage](https://recalls-rappels.canada.ca/en/alert-recall/cadd-solis-ambulatory-infusion-pump) for more details and updates regarding this critical recall affecting the CADD-Solis Ambulatory Infusion Pump.